8ROK: Structural maintenance of chromosomes protein 3

Human cohesin SMC3-HD(EQ)/RAD21-N complex - ATP-Mg-bound conformation - Form 1. Determined by X-ray diffraction at 2.25 Å resolution. Released 11 Sept 2024.

Method
X-ray diffraction
Resolution
2.25 Å
Organism
Homo sapiens
Chains
4
Atoms
7,683
Mol. weight
131.11 kDa
Ligands
MG, AGS
Released
11 Sept 2024

Explore 8ROK in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

8ROK contains 41 α-helices and 36 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 16 helices, 18 β-strands

ElementResiduesLengthSheet
β-strand2-981
β-strand1112
β-strand1412
β-strand18-1921
α-helix20-245
β-strand27-3153
α-helix38-4912
α-helix51-533
α-helix58-647
β-strand6512
α-helix72-732
β-strand75-8391
β-strand95-10391
β-strand107-11151
β-strand114-11631
α-helix118-12710
β-strand138-14033
α-helix141-1488
α-helix152-16312
α-helix165-19026
α-helix191-1944
α-helix995-104753
β-strand1052-105764
β-strand1096-110164
β-strand1110-111124
α-helix1112-11143
α-helix1117-113216
β-strand1139-114353
α-helix1151-116414
β-strand1169-117353
α-helix1180-11823
β-strand1185-119283
β-strand1195-120173
α-helix1203-12108
Chain B: 5 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix13-2210
α-helix24-263
α-helix29-346
α-helix37-459
α-helix53-7927
Chain C: 16 helices, 18 β-strands
ElementResiduesLengthSheet
β-strand2-985
β-strand1116
β-strand1416
β-strand18-1925
α-helix22-243
β-strand27-3157
α-helix38-4912
α-helix51-533
α-helix58-647
β-strand6516
α-helix72-732
β-strand75-8395
β-strand95-10395
β-strand107-11155
β-strand114-11635
α-helix118-12710
β-strand138-14037
α-helix141-1488
α-helix152-16312
α-helix165-19935
α-helix992-102332
α-helix1025-104723
β-strand1052-105768
β-strand1096-110168
β-strand1110-111128
α-helix1112-11143
α-helix1117-113418
β-strand1139-114357
α-helix1151-116414
β-strand1169-117357
α-helix1179-11824
β-strand1185-119287
β-strand1195-120177
α-helix1203-12119
Chain D: 4 helices, 0 β-strands
ElementResiduesLengthSheet
α-helix12-2211
α-helix29-346
α-helix37-459
α-helix53-8634

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Structural maintenance of chromosomes protein 3A, Cprotein462Homo sapiensQ9UQE7 (AlphaFold model)
Double-strand-break repair protein rad21 homologB, Dprotein110Homo sapiensO60216 (AlphaFold model)
Sequence of entity 1 (A, C), FASTA
>8ROK_1 Structural maintenance of chromosomes protein 3 (chains A, C)
MYIKQVIIQGFRSYRDQTIVDPFSSKHNVIVGRNGSGKSNFFYAIQFVLSDEFSHLRPEQ
RLALLHEGTGPRVISAFVEIIFDNSDNRLPIDKEEVSLRRVIGAKKDQYFLDKKMVTKND
VMNLLESAGFSRSNPYYIVKQGKINQMATAPDSQRLKLLREVAGTRVYDERKEESISLMK
ETEGKREKINELLKYIEERLHTLEEEKEELAGSGSLVPRGSGSYSHVNKKALDQFVNFSE
QKEKLIKRQEELDRGYKSIMELMNVLELRKYEAIQLTFKQVSKNFSEVFQKLVPGGKATL
VMKKGDVEGSQSQDEGEGSGESERGSGSQSSVPSVDQFTGVGIRVSFTGKQGEMREMQQL
SGGQKSLVALALIFAIQKCDPAPFYLFDQIDQALDAQHRKAVSDMIMELAVHAQFITTTF
RPELLESADKFYGVKFRNKVSHIDVITAEMAKDFVEDDTTHG
Sequence of entity 2 (B, D), FASTA
>8ROK_2 Double-strand-break repair protein rad21 homolog (chains B, D)
MFYAHFVLSKRGPLAKIWLAAHWDKKLTKAHVFECNLESSVESIISPKVKMALRTSGHLL
LGVVRIYHRKAKYLLADCNEAFIKIKMAFRPGVVDLPEENREGSLEVLFQ

Ligands and cofactors

IDNameFormulaCopies
MGMagnesium ionMg2
AGSPhosphothiophosphoric acid-adenylate esterC10 H16 N5 O12 P3 S2

Primary citation

The cohesin ATPase cycle is mediated by specific conformational dynamics and interface plasticity of SMC1A and SMC3 ATPase domains. Vitoria Gomes, M., Landwerlin, P., Diebold-Durand, M.L. et al. Cell Rep (2024) 43:114656-114656. DOI 10.1016/j.celrep.2024.114656 · PubMed

Other PDB entries of the same protein (UniProt Q9UQE7 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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