3TVJ: Catalytic fragment of MASP-2

Catalytic fragment of MASP-2 in complex with its specific inhibitor developed by directed evolution on SGCI scaffold. Determined by X-ray diffraction at 1.28 Å resolution. Released 25 Apr 2012.

Method
X-ray diffraction
Resolution
1.28 Å
Organisms
Homo sapiens, Schistocerca gregaria
Chains
3
Atoms
3,450
Mol. weight
39.88 kDa
Released
25 Apr 2012

Explore 3TVJ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3TVJ contains 18 α-helices and 32 β-strands across 3 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: 4 helices, 8 β-strands

ElementResiduesLengthSheet
β-strand36511
α-helix369-3713
β-strand375-37952
β-strand38711
β-strand391-39662
α-helix3971
β-strand401-40443
β-strand409-41242
β-strand418-42032
α-helix427-4282
β-strand429-43243
α-helix433-4342
Chain B: 14 helices, 20 β-strands
ElementResiduesLengthSheet
β-strand44614
β-strand449-45025
α-helix451-4522
β-strand459-46356
β-strand466-47276
β-strand477-48046
α-helix482-4854
α-helix486-4905
α-helix494-4952
β-strand496-49946
β-strand50317
α-helix5091
β-strand510-519106
β-strand534-53856
α-helix541-5444
β-strand54518
β-strand54818
α-helix550-5512
β-strand55215
α-helix553-5542
α-helix558-5614
β-strand567-57265
β-strand58417
β-strand586-59275
α-helix593-5942
α-helix595-6039
α-helix6081
β-strand616-61945
β-strand62714
β-strand636-64165
β-strand646-657125
β-strand667-67155
α-helix672-6754
α-helix676-68510
Chain I: 0 helices, 4 β-strands
ElementResiduesLengthSheet
β-strand9-1245
β-strand15-1955
β-strand26-2945
β-strand32-3326

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Mannan-binding lectin serine protease 2 A chainAprotein86Homo sapiensO00187 (AlphaFold model)
Mannan-binding lectin serine protease 2 B chainBprotein242Homo sapiensO00187 (AlphaFold model)
Protease inhibitor SGPI-2Iprotein38Schistocerca gregariaO46162 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>3TVJ_1 Mannan-binding lectin serine protease 2 A chain (chains A)
ASMTIVDCGPPDDLPSGRVEYITGPGVTTYKAVIQYSCEETFYTMKVNDGKYVCDADGFW
TSSKGEKSLPVCEPVCGLSARTTGGR
Sequence of entity 2 (B), FASTA
>3TVJ_2 Mannan-binding lectin serine protease 2 B chain (chains B)
IYGGQKAKPGDFPWQVLILGGTTAAGALLYDNWVLTAAHAVYEQKHDASALDIRMGTLKR
LSPHYTQAWSEAVFIHEGYTHDAGFDNDIALIKLNNKVVINSNITPICLPRKEAESFMRT
DDIGTASGWGLTQRGFLARNLMYVDIPIVDHQKCTAAYEKPPYPRGSVTANMLCAGLESG
GKDSCRGDSGGALVFLDSETERWFVGGIVSWGSMNCGEAGQYGVYTKVINYIPWIENIIS
DF
Sequence of entity 3 (I), FASTA
>3TVJ_3 Protease inhibitor SGPI-2 (chains I)
GSGEVTCEPGTTFKDKCNTCRCGSDGKSAVCTKLWCNQ

Primary citation

Monospecific Inhibitors Show That Both Mannan-binding Lectin-associated Serine Protease-1 (MASP-1) and -2 Are Essential for Lectin Pathway Activation and Reveal Structural Plasticity of MASP-2. Heja, D., Harmat, V., Fodor, K. et al. J Biol Chem (2012) 287:20290-20300. DOI 10.1074/jbc.M112.354332 · PubMed

Other PDB entries of the same protein (UniProt O00187 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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