LeishMANIAdb
  • Home
  • Browse
  • Manual
  • FAQ
  • Download

Phosphoglycan_beta_1_-3_galactosyltransferase

Quick info Annotations Function or PPIs Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Phosphoglycan_beta_1_-3_galactosyltransferase
Gene product:
hypothetical protein
Species:
Leishmania mexicana
UniProt:
E9AJI4_LEIMU
TriTrypDb:
LmxM.02.0170
Length:
798

Annotations

LeishMANIAdb annotations

Phosphoglycan beta 1,3 galactosyltransferase (required for proper protective coat formation). Probably part of a much larger group. Expanded in Leishmaniids. Localization: Golgi (by homology)

Localization

Secreted promastigote
Source Evidence on protein Close homologs
Cuervo et al. no yes: 0
Hassani et al. no yes: 0
Forrest at al. (metacyclic) no yes: 0
Forrest at al. (procyclic) no yes: 0
Silverman et al. no yes: 0
Pissara et al. yes yes: 60
Secreted amastigote
Source Evidence on protein Close homologs
Pires et al. no yes: 0
Exosome
Source Evidence on protein Close homologs
Silverman et al. no yes: 0
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 16
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 52
NetGPI no yes: 0, no: 52
Cellular components
Term Name Level Count
GO:0016020 membrane 2 53
GO:0110165 cellular anatomical entity 1 53
GO:0000139 Golgi membrane 5 14
GO:0031090 organelle membrane 3 14
GO:0098588 bounding membrane of organelle 4 14

Expansion

Sequence features

E9AJI4
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AJI4

Function

Biological processes
Term Name Level Count
GO:0006486 protein glycosylation 4 53
GO:0006807 nitrogen compound metabolic process 2 53
GO:0008152 metabolic process 1 53
GO:0019538 protein metabolic process 3 53
GO:0036211 protein modification process 4 53
GO:0043170 macromolecule metabolic process 3 53
GO:0043412 macromolecule modification 4 53
GO:0043413 macromolecule glycosylation 3 53
GO:0044238 primary metabolic process 2 53
GO:0070085 glycosylation 2 53
GO:0071704 organic substance metabolic process 2 53
GO:1901564 organonitrogen compound metabolic process 3 53
Molecular functions
Term Name Level Count
GO:0003824 catalytic activity 1 53
GO:0016740 transferase activity 2 53
GO:0016757 glycosyltransferase activity 3 53
GO:0016758 hexosyltransferase activity 4 53
GO:0008194 UDP-glycosyltransferase activity 4 14

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 259 263 PF00656 0.408
CLV_C14_Caspase3-7 341 345 PF00656 0.495
CLV_C14_Caspase3-7 385 389 PF00656 0.423
CLV_NRD_NRD_1 129 131 PF00675 0.680
CLV_NRD_NRD_1 394 396 PF00675 0.731
CLV_NRD_NRD_1 399 401 PF00675 0.727
CLV_NRD_NRD_1 477 479 PF00675 0.728
CLV_NRD_NRD_1 577 579 PF00675 0.554
CLV_NRD_NRD_1 59 61 PF00675 0.500
CLV_NRD_NRD_1 737 739 PF00675 0.594
CLV_NRD_NRD_1 786 788 PF00675 0.586
CLV_NRD_NRD_1 84 86 PF00675 0.522
CLV_NRD_NRD_1 88 90 PF00675 0.522
CLV_PCSK_FUR_1 57 61 PF00082 0.449
CLV_PCSK_KEX2_1 117 119 PF00082 0.674
CLV_PCSK_KEX2_1 129 131 PF00082 0.662
CLV_PCSK_KEX2_1 352 354 PF00082 0.694
CLV_PCSK_KEX2_1 394 396 PF00082 0.729
CLV_PCSK_KEX2_1 399 401 PF00082 0.725
CLV_PCSK_KEX2_1 477 479 PF00082 0.657
CLV_PCSK_KEX2_1 547 549 PF00082 0.623
CLV_PCSK_KEX2_1 577 579 PF00082 0.560
CLV_PCSK_KEX2_1 59 61 PF00082 0.486
CLV_PCSK_KEX2_1 650 652 PF00082 0.595
CLV_PCSK_KEX2_1 736 738 PF00082 0.582
CLV_PCSK_KEX2_1 760 762 PF00082 0.603
CLV_PCSK_KEX2_1 786 788 PF00082 0.605
CLV_PCSK_KEX2_1 83 85 PF00082 0.536
CLV_PCSK_KEX2_1 90 92 PF00082 0.516
CLV_PCSK_PC1ET2_1 117 119 PF00082 0.640
CLV_PCSK_PC1ET2_1 352 354 PF00082 0.652
CLV_PCSK_PC1ET2_1 547 549 PF00082 0.587
CLV_PCSK_PC1ET2_1 650 652 PF00082 0.526
CLV_PCSK_PC1ET2_1 736 738 PF00082 0.560
CLV_PCSK_PC1ET2_1 760 762 PF00082 0.601
CLV_PCSK_PC1ET2_1 90 92 PF00082 0.477
CLV_PCSK_PC7_1 395 401 PF00082 0.604
CLV_PCSK_PC7_1 646 652 PF00082 0.556
CLV_PCSK_PC7_1 782 788 PF00082 0.562
CLV_PCSK_PC7_1 80 86 PF00082 0.458
CLV_PCSK_SKI1_1 114 118 PF00082 0.615
CLV_PCSK_SKI1_1 288 292 PF00082 0.621
CLV_PCSK_SKI1_1 367 371 PF00082 0.622
CLV_PCSK_SKI1_1 418 422 PF00082 0.597
CLV_PCSK_SKI1_1 460 464 PF00082 0.495
CLV_PCSK_SKI1_1 502 506 PF00082 0.637
CLV_PCSK_SKI1_1 632 636 PF00082 0.522
CLV_PCSK_SKI1_1 650 654 PF00082 0.531
DEG_APCC_DBOX_1 352 360 PF00400 0.453
DEG_ODPH_VHL_1 602 615 PF01847 0.354
DEG_SCF_FBW7_1 438 445 PF00400 0.516
DEG_SCF_FBW7_2 407 414 PF00400 0.377
DEG_SPOP_SBC_1 11 15 PF00917 0.632
DOC_CKS1_1 213 218 PF01111 0.376
DOC_CKS1_1 270 275 PF01111 0.394
DOC_CKS1_1 439 444 PF01111 0.518
DOC_CYCLIN_yCln2_LP_2 436 442 PF00134 0.562
DOC_MAPK_gen_1 577 585 PF00069 0.345
DOC_MAPK_gen_1 89 95 PF00069 0.717
DOC_MAPK_JIP1_4 91 97 PF00069 0.507
DOC_MAPK_MEF2A_6 222 230 PF00069 0.398
DOC_MAPK_MEF2A_6 466 473 PF00069 0.481
DOC_MAPK_MEF2A_6 490 499 PF00069 0.376
DOC_MAPK_MEF2A_6 89 97 PF00069 0.748
DOC_PP1_RVXF_1 30 37 PF00149 0.658
DOC_PP1_RVXF_1 464 471 PF00149 0.380
DOC_PP1_RVXF_1 500 507 PF00149 0.476
DOC_PP1_RVXF_1 658 664 PF00149 0.319
DOC_PP2B_LxvP_1 436 439 PF13499 0.565
DOC_PP2B_LxvP_1 549 552 PF13499 0.330
DOC_PP4_FxxP_1 165 168 PF00568 0.399
DOC_PP4_FxxP_1 444 447 PF00568 0.403
DOC_USP7_MATH_1 12 16 PF00917 0.644
DOC_USP7_MATH_1 229 233 PF00917 0.388
DOC_USP7_MATH_1 294 298 PF00917 0.340
DOC_USP7_MATH_1 387 391 PF00917 0.416
DOC_USP7_MATH_1 424 428 PF00917 0.451
DOC_USP7_MATH_1 58 62 PF00917 0.665
DOC_WW_Pin1_4 164 169 PF00397 0.434
DOC_WW_Pin1_4 212 217 PF00397 0.378
DOC_WW_Pin1_4 269 274 PF00397 0.433
DOC_WW_Pin1_4 335 340 PF00397 0.507
DOC_WW_Pin1_4 407 412 PF00397 0.570
DOC_WW_Pin1_4 438 443 PF00397 0.522
DOC_WW_Pin1_4 690 695 PF00397 0.356
DOC_WW_Pin1_4 759 764 PF00397 0.399
LIG_14-3-3_CanoR_1 17 21 PF00244 0.642
LIG_14-3-3_CanoR_1 170 177 PF00244 0.404
LIG_14-3-3_CanoR_1 194 201 PF00244 0.478
LIG_14-3-3_CanoR_1 296 300 PF00244 0.521
LIG_14-3-3_CanoR_1 32 37 PF00244 0.677
LIG_14-3-3_CanoR_1 353 361 PF00244 0.441
LIG_14-3-3_CanoR_1 418 423 PF00244 0.472
LIG_14-3-3_CanoR_1 737 745 PF00244 0.393
LIG_Actin_WH2_2 157 172 PF00022 0.412
LIG_Actin_WH2_2 236 252 PF00022 0.425
LIG_BIR_II_1 1 5 PF00653 0.665
LIG_BRCT_BRCA1_1 171 175 PF00533 0.383
LIG_EH1_1 590 598 PF00400 0.300
LIG_eIF4E_1 102 108 PF01652 0.292
LIG_FHA_1 178 184 PF00498 0.564
LIG_FHA_1 232 238 PF00498 0.546
LIG_FHA_1 270 276 PF00498 0.393
LIG_FHA_1 368 374 PF00498 0.422
LIG_FHA_1 40 46 PF00498 0.691
LIG_FHA_1 424 430 PF00498 0.469
LIG_FHA_1 588 594 PF00498 0.339
LIG_FHA_1 634 640 PF00498 0.283
LIG_FHA_2 257 263 PF00498 0.389
LIG_FHA_2 299 305 PF00498 0.458
LIG_FHA_2 360 366 PF00498 0.537
LIG_FHA_2 376 382 PF00498 0.445
LIG_FHA_2 49 55 PF00498 0.676
LIG_FHA_2 633 639 PF00498 0.324
LIG_FHA_2 691 697 PF00498 0.342
LIG_IRF3_LxIS_1 165 172 PF10401 0.395
LIG_LIR_Apic_2 163 168 PF02991 0.399
LIG_LIR_Apic_2 441 447 PF02991 0.408
LIG_LIR_Apic_2 488 494 PF02991 0.497
LIG_LIR_Gen_1 272 281 PF02991 0.383
LIG_LIR_Gen_1 301 306 PF02991 0.375
LIG_LIR_Gen_1 508 519 PF02991 0.408
LIG_LIR_Gen_1 525 535 PF02991 0.403
LIG_LIR_Gen_1 681 689 PF02991 0.431
LIG_LIR_Gen_1 696 704 PF02991 0.334
LIG_LIR_Gen_1 791 798 PF02991 0.330
LIG_LIR_Nem_3 215 220 PF02991 0.373
LIG_LIR_Nem_3 255 260 PF02991 0.420
LIG_LIR_Nem_3 272 277 PF02991 0.393
LIG_LIR_Nem_3 297 302 PF02991 0.519
LIG_LIR_Nem_3 508 514 PF02991 0.456
LIG_LIR_Nem_3 525 531 PF02991 0.366
LIG_LIR_Nem_3 638 644 PF02991 0.340
LIG_LIR_Nem_3 681 687 PF02991 0.436
LIG_LIR_Nem_3 696 700 PF02991 0.334
LIG_LIR_Nem_3 791 797 PF02991 0.369
LIG_Pex14_2 175 179 PF04695 0.384
LIG_REV1ctd_RIR_1 701 710 PF16727 0.335
LIG_SH2_CRK 213 217 PF00017 0.380
LIG_SH2_CRK 528 532 PF00017 0.294
LIG_SH2_CRK 697 701 PF00017 0.307
LIG_SH2_NCK_1 213 217 PF00017 0.380
LIG_SH2_NCK_1 765 769 PF00017 0.409
LIG_SH2_SRC 302 305 PF00017 0.388
LIG_SH2_SRC 509 512 PF00017 0.410
LIG_SH2_SRC 699 702 PF00017 0.321
LIG_SH2_STAP1 509 513 PF00017 0.499
LIG_SH2_STAP1 562 566 PF00017 0.363
LIG_SH2_STAP1 765 769 PF00017 0.382
LIG_SH2_STAT5 102 105 PF00017 0.313
LIG_SH2_STAT5 274 277 PF00017 0.436
LIG_SH2_STAT5 320 323 PF00017 0.462
LIG_SH2_STAT5 431 434 PF00017 0.417
LIG_SH2_STAT5 450 453 PF00017 0.477
LIG_SH2_STAT5 540 543 PF00017 0.413
LIG_SH2_STAT5 699 702 PF00017 0.494
LIG_SH2_STAT5 780 783 PF00017 0.381
LIG_SH3_1 213 219 PF00018 0.375
LIG_SH3_3 213 219 PF00018 0.380
LIG_SH3_3 267 273 PF00018 0.499
LIG_SH3_3 27 33 PF00018 0.647
LIG_SH3_3 436 442 PF00018 0.562
LIG_SH3_3 5 11 PF00018 0.652
LIG_SH3_3 598 604 PF00018 0.373
LIG_SH3_3 792 798 PF00018 0.334
LIG_SUMO_SIM_anti_2 104 110 PF11976 0.319
LIG_SUMO_SIM_anti_2 612 617 PF11976 0.345
LIG_SUMO_SIM_par_1 612 617 PF11976 0.347
LIG_TRAF2_1 301 304 PF00917 0.402
LIG_TYR_ITIM 300 305 PF00017 0.593
LIG_TYR_ITSM 270 277 PF00017 0.443
LIG_UBA3_1 112 117 PF00899 0.447
LIG_WRC_WIRS_1 20 25 PF05994 0.512
LIG_WW_3 268 272 PF00397 0.469
MOD_CDC14_SPxK_1 167 170 PF00782 0.487
MOD_CDK_SPxK_1 164 170 PF00069 0.486
MOD_CK1_1 155 161 PF00069 0.470
MOD_CK1_1 19 25 PF00069 0.611
MOD_CK1_1 238 244 PF00069 0.379
MOD_CK1_1 338 344 PF00069 0.718
MOD_CK1_1 35 41 PF00069 0.607
MOD_CK1_1 4 10 PF00069 0.556
MOD_CK1_1 427 433 PF00069 0.470
MOD_CK1_1 48 54 PF00069 0.641
MOD_CK1_1 576 582 PF00069 0.378
MOD_CK1_1 61 67 PF00069 0.482
MOD_CK2_1 196 202 PF00069 0.555
MOD_CK2_1 298 304 PF00069 0.541
MOD_CK2_1 344 350 PF00069 0.625
MOD_CK2_1 359 365 PF00069 0.684
MOD_CK2_1 375 381 PF00069 0.502
MOD_CK2_1 443 449 PF00069 0.474
MOD_CK2_1 48 54 PF00069 0.596
MOD_CK2_1 564 570 PF00069 0.406
MOD_GlcNHglycan 1 4 PF01048 0.546
MOD_GlcNHglycan 171 174 PF01048 0.502
MOD_GlcNHglycan 198 201 PF01048 0.678
MOD_GlcNHglycan 340 343 PF01048 0.684
MOD_GlcNHglycan 346 349 PF01048 0.586
MOD_GlcNHglycan 356 359 PF01048 0.540
MOD_GlcNHglycan 425 429 PF01048 0.519
MOD_GlcNHglycan 432 435 PF01048 0.568
MOD_GlcNHglycan 455 458 PF01048 0.607
MOD_GlcNHglycan 559 562 PF01048 0.501
MOD_GlcNHglycan 605 608 PF01048 0.449
MOD_GlcNHglycan 625 628 PF01048 0.343
MOD_GSK3_1 12 19 PF00069 0.537
MOD_GSK3_1 151 158 PF00069 0.506
MOD_GSK3_1 160 167 PF00069 0.502
MOD_GSK3_1 189 196 PF00069 0.548
MOD_GSK3_1 231 238 PF00069 0.360
MOD_GSK3_1 294 301 PF00069 0.335
MOD_GSK3_1 32 39 PF00069 0.631
MOD_GSK3_1 334 341 PF00069 0.730
MOD_GSK3_1 414 421 PF00069 0.607
MOD_GSK3_1 423 430 PF00069 0.521
MOD_GSK3_1 434 441 PF00069 0.528
MOD_GSK3_1 44 51 PF00069 0.686
MOD_GSK3_1 628 635 PF00069 0.339
MOD_GSK3_1 708 715 PF00069 0.449
MOD_GSK3_1 755 762 PF00069 0.374
MOD_GSK3_1 778 785 PF00069 0.389
MOD_N-GLC_1 151 156 PF02516 0.503
MOD_N-GLC_1 39 44 PF02516 0.568
MOD_NEK2_1 1 6 PF00069 0.557
MOD_NEK2_1 101 106 PF00069 0.415
MOD_NEK2_1 151 156 PF00069 0.619
MOD_NEK2_1 16 21 PF00069 0.580
MOD_NEK2_1 169 174 PF00069 0.444
MOD_NEK2_1 228 233 PF00069 0.437
MOD_NEK2_1 36 41 PF00069 0.601
MOD_NEK2_1 45 50 PF00069 0.606
MOD_NEK2_1 485 490 PF00069 0.525
MOD_NEK2_1 542 547 PF00069 0.471
MOD_NEK2_1 557 562 PF00069 0.491
MOD_NEK2_1 628 633 PF00069 0.352
MOD_NEK2_1 708 713 PF00069 0.413
MOD_NEK2_2 12 17 PF00069 0.521
MOD_NEK2_2 177 182 PF00069 0.694
MOD_NEK2_2 755 760 PF00069 0.354
MOD_PIKK_1 152 158 PF00454 0.522
MOD_PIKK_1 497 503 PF00454 0.597
MOD_PIKK_1 542 548 PF00454 0.401
MOD_PKA_1 477 483 PF00069 0.651
MOD_PKA_1 736 742 PF00069 0.427
MOD_PKA_1 83 89 PF00069 0.479
MOD_PKA_2 16 22 PF00069 0.538
MOD_PKA_2 169 175 PF00069 0.460
MOD_PKA_2 193 199 PF00069 0.592
MOD_PKA_2 295 301 PF00069 0.632
MOD_PKA_2 375 381 PF00069 0.462
MOD_PKA_2 477 483 PF00069 0.565
MOD_PKA_2 576 582 PF00069 0.354
MOD_PKA_2 58 64 PF00069 0.575
MOD_PKA_2 736 742 PF00069 0.442
MOD_PKA_2 781 787 PF00069 0.468
MOD_PKA_2 83 89 PF00069 0.511
MOD_Plk_1 235 241 PF00069 0.375
MOD_Plk_1 387 393 PF00069 0.436
MOD_Plk_1 424 430 PF00069 0.475
MOD_Plk_1 524 530 PF00069 0.414
MOD_Plk_1 680 686 PF00069 0.453
MOD_Plk_4 160 166 PF00069 0.510
MOD_Plk_4 295 301 PF00069 0.544
MOD_Plk_4 387 393 PF00069 0.500
MOD_Plk_4 427 433 PF00069 0.458
MOD_Plk_4 524 530 PF00069 0.418
MOD_Plk_4 587 593 PF00069 0.378
MOD_Plk_4 683 689 PF00069 0.555
MOD_ProDKin_1 164 170 PF00069 0.511
MOD_ProDKin_1 212 218 PF00069 0.425
MOD_ProDKin_1 269 275 PF00069 0.496
MOD_ProDKin_1 335 341 PF00069 0.611
MOD_ProDKin_1 407 413 PF00069 0.697
MOD_ProDKin_1 438 444 PF00069 0.625
MOD_ProDKin_1 690 696 PF00069 0.396
MOD_ProDKin_1 759 765 PF00069 0.455
TRG_DiLeu_BaLyEn_6 592 597 PF01217 0.448
TRG_ENDOCYTIC_2 274 277 PF00928 0.511
TRG_ENDOCYTIC_2 302 305 PF00928 0.632
TRG_ENDOCYTIC_2 511 514 PF00928 0.614
TRG_ENDOCYTIC_2 528 531 PF00928 0.313
TRG_ENDOCYTIC_2 697 700 PF00928 0.336
TRG_ER_diArg_1 128 130 PF00400 0.505
TRG_ER_diArg_1 394 396 PF00400 0.635
TRG_ER_diArg_1 398 400 PF00400 0.607
TRG_ER_diArg_1 477 479 PF00400 0.506
TRG_ER_diArg_1 57 60 PF00400 0.565
TRG_ER_diArg_1 668 671 PF00400 0.412
TRG_ER_diArg_1 786 788 PF00400 0.458
TRG_ER_diArg_1 82 85 PF00400 0.614
TRG_ER_diArg_1 88 91 PF00400 0.625
TRG_Pf-PMV_PEXEL_1 595 599 PF00026 0.497
TRG_Pf-PMV_PEXEL_1 786 791 PF00026 0.395

Homologs

Protein Taxonomy Sequence identity Coverage
A0A3Q8IGN9 Leishmania donovani 40% 98%
A0A3S5H4Y6 Leishmania donovani 80% 99%
A0A3S5H4Y9 Leishmania donovani 35% 80%
A0A3S7WT86 Leishmania donovani 42% 78%
A0A3S7WWA6 Leishmania donovani 40% 98%
A0A451EJD9 Leishmania donovani 40% 98%
A0A451EJF4 Leishmania donovani 70% 98%
A0A451EJF6 Leishmania donovani 69% 100%
A0A451EJF8 Leishmania donovani 59% 100%
A0A451EJF9 Leishmania donovani 59% 92%
A4H3A9 Leishmania braziliensis 62% 100%
A4H3B4 Leishmania braziliensis 61% 100%
A4H3B6 Leishmania braziliensis 62% 100%
A4H3B8 Leishmania braziliensis 61% 100%
A4H3B9 Leishmania braziliensis 40% 100%
A4H4W8 Leishmania braziliensis 38% 100%
A4HJ20 Leishmania braziliensis 59% 100%
A4HNK3 Leishmania braziliensis 41% 99%
A4HNK6 Leishmania braziliensis 38% 100%
A4HRL9 Leishmania infantum 71% 98%
A4HRM0 Leishmania infantum 75% 100%
A4HRM1 Leishmania infantum 69% 100%
A4HRS1 Leishmania infantum 58% 92%
A4HRS3 Leishmania infantum 35% 80%
A4HRS5 Leishmania infantum 59% 100%
A4HZM0 Leishmania infantum 39% 98%
A4I7C7 Leishmania infantum 40% 98%
A4IAQ2 Leishmania infantum 39% 98%
E9AC91 Leishmania major 71% 100%
E9AC92 Leishmania major 72% 100%
E9AC94 Leishmania major 35% 100%
E9AC95 Leishmania major 58% 98%
E9AC96 Leishmania major 62% 100%
E9AC98 Leishmania major 35% 100%
E9AEH8 Leishmania major 42% 100%
E9AHA6 Leishmania infantum 39% 98%
E9AIP8 Leishmania braziliensis 40% 100%
E9AJI3 Leishmania mexicana (strain MHOM/GT/2001/U1103) 90% 98%
E9AJI5 Leishmania mexicana (strain MHOM/GT/2001/U1103) 62% 100%
E9AJI6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 37% 81%
E9ALD6 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 100%
E9ASB8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 98%
E9AXX8 Leishmania mexicana (strain MHOM/GT/2001/U1103) 40% 98%
E9B2C0 Leishmania mexicana (strain MHOM/GT/2001/U1103) 41% 98%
Q4Q5T6 Leishmania major 40% 100%
Q4QCL8 Leishmania major 39% 100%
Q4QFJ3 Leishmania major 43% 100%
Q4QIG9 Leishmania major 40% 100%
Q7YXU9 Leishmania major 42% 100%
Q7YXV1 Leishmania major 39% 100%
Q7YXV2 Leishmania major 41% 100%

Download

Download
LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2024 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS