LeishMANIAdb
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Uncharacterized protein

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

Quick info

Protein:
Uncharacterized protein
Gene product:
hypothetical protein - conserved
Species:
Leishmania infantum
UniProt:
A4HZW6_LEIIN
TriTrypDb:
LINF_220015200
Length:
884

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. no yes: 0
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: 0
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 1, no: 5
NetGPI no yes: 0, no: 6
Cellular components
Term Name Level Count
GO:0032991 protein-containing complex 1 1
GO:0034702 monoatomic ion channel complex 4 1
GO:0034703 cation channel complex 5 1
GO:0034704 calcium channel complex 6 1
GO:0098796 membrane protein complex 2 1
GO:0098798 mitochondrial protein-containing complex 2 1
GO:0098800 inner mitochondrial membrane protein complex 3 1
GO:1902495 transmembrane transporter complex 3 1
GO:1990246 uniplex complex 4 1
GO:1990351 transporter complex 2 1

Expansion

Sequence features

A4HZW6
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HZW6

Function

Biological processes
Term Name Level Count
GO:0006810 transport 3 7
GO:0006811 monoatomic ion transport 4 7
GO:0006812 monoatomic cation transport 5 7
GO:0006816 calcium ion transport 7 7
GO:0006851 mitochondrial calcium ion transmembrane transport 4 7
GO:0009987 cellular process 1 7
GO:0030001 metal ion transport 6 7
GO:0034220 monoatomic ion transmembrane transport 3 7
GO:0051179 localization 1 7
GO:0051234 establishment of localization 2 7
GO:0055085 transmembrane transport 2 7
GO:0070588 calcium ion transmembrane transport 6 7
GO:0098655 monoatomic cation transmembrane transport 4 7
GO:0098660 inorganic ion transmembrane transport 4 7
GO:0098662 inorganic cation transmembrane transport 5 7
GO:1990542 mitochondrial transmembrane transport 3 7
GO:0006873 intracellular monoatomic ion homeostasis 4 1
GO:0006874 intracellular calcium ion homeostasis 7 1
GO:0006875 obsolete intracellular metal ion homeostasis 6 1
GO:0019725 cellular homeostasis 2 1
GO:0030003 intracellular monoatomic cation homeostasis 5 1
GO:0036444 calcium import into the mitochondrion 5 1
GO:0042592 homeostatic process 3 1
GO:0048878 chemical homeostasis 4 1
GO:0050801 monoatomic ion homeostasis 5 1
GO:0051560 mitochondrial calcium ion homeostasis 8 1
GO:0055065 obsolete metal ion homeostasis 7 1
GO:0055074 calcium ion homeostasis 8 1
GO:0055080 monoatomic cation homeostasis 6 1
GO:0055082 intracellular chemical homeostasis 3 1
GO:0065007 biological regulation 1 1
GO:0065008 regulation of biological quality 2 1
GO:0072503 obsolete cellular divalent inorganic cation homeostasis 6 1
GO:0072507 obsolete divalent inorganic cation homeostasis 7 1
GO:0098771 inorganic ion homeostasis 6 1
Molecular functions
Term Name Level Count
GO:0005488 binding 1 7
GO:0005509 calcium ion binding 5 7
GO:0043167 ion binding 2 7
GO:0043169 cation binding 3 7
GO:0046872 metal ion binding 4 7

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 63 67 PF00656 0.575
CLV_C14_Caspase3-7 774 778 PF00656 0.636
CLV_C14_Caspase3-7 837 841 PF00656 0.532
CLV_NRD_NRD_1 230 232 PF00675 0.619
CLV_NRD_NRD_1 373 375 PF00675 0.552
CLV_NRD_NRD_1 427 429 PF00675 0.696
CLV_NRD_NRD_1 433 435 PF00675 0.627
CLV_NRD_NRD_1 44 46 PF00675 0.566
CLV_NRD_NRD_1 477 479 PF00675 0.555
CLV_NRD_NRD_1 636 638 PF00675 0.471
CLV_NRD_NRD_1 644 646 PF00675 0.454
CLV_PCSK_KEX2_1 197 199 PF00082 0.397
CLV_PCSK_KEX2_1 230 232 PF00082 0.619
CLV_PCSK_KEX2_1 327 329 PF00082 0.426
CLV_PCSK_KEX2_1 373 375 PF00082 0.552
CLV_PCSK_KEX2_1 427 429 PF00082 0.696
CLV_PCSK_KEX2_1 433 435 PF00082 0.627
CLV_PCSK_KEX2_1 44 46 PF00082 0.566
CLV_PCSK_KEX2_1 636 638 PF00082 0.471
CLV_PCSK_KEX2_1 644 646 PF00082 0.454
CLV_PCSK_KEX2_1 869 871 PF00082 0.599
CLV_PCSK_PC1ET2_1 197 199 PF00082 0.397
CLV_PCSK_PC1ET2_1 327 329 PF00082 0.441
CLV_PCSK_PC1ET2_1 869 871 PF00082 0.599
CLV_PCSK_PC7_1 640 646 PF00082 0.517
CLV_PCSK_SKI1_1 214 218 PF00082 0.373
CLV_PCSK_SKI1_1 327 331 PF00082 0.433
CLV_PCSK_SKI1_1 456 460 PF00082 0.399
CLV_PCSK_SKI1_1 479 483 PF00082 0.541
CLV_PCSK_SKI1_1 5 9 PF00082 0.551
CLV_PCSK_SKI1_1 537 541 PF00082 0.541
CLV_PCSK_SKI1_1 636 640 PF00082 0.426
CLV_PCSK_SKI1_1 645 649 PF00082 0.525
CLV_PCSK_SKI1_1 689 693 PF00082 0.412
CLV_PCSK_SKI1_1 792 796 PF00082 0.551
CLV_PCSK_SKI1_1 827 831 PF00082 0.509
CLV_PCSK_SKI1_1 854 858 PF00082 0.562
CLV_Separin_Metazoa 453 457 PF03568 0.471
CLV_Separin_Metazoa 722 726 PF03568 0.479
DEG_APCC_DBOX_1 536 544 PF00400 0.526
DEG_APCC_DBOX_1 610 618 PF00400 0.371
DEG_APCC_DBOX_1 688 696 PF00400 0.452
DEG_SCF_FBW7_1 319 325 PF00400 0.455
DEG_SCF_FBW7_1 543 549 PF00400 0.603
DEG_SCF_TRCP1_1 239 244 PF00400 0.573
DEG_SCF_TRCP1_1 337 342 PF00400 0.327
DOC_CDC14_PxL_1 597 605 PF14671 0.390
DOC_CKS1_1 319 324 PF01111 0.494
DOC_CKS1_1 407 412 PF01111 0.590
DOC_CKS1_1 543 548 PF01111 0.602
DOC_CYCLIN_RxL_1 531 541 PF00134 0.535
DOC_CYCLIN_RxL_1 827 837 PF00134 0.509
DOC_CYCLIN_yClb1_LxF_4 35 40 PF00134 0.539
DOC_CYCLIN_yCln2_LP_2 454 460 PF00134 0.481
DOC_MAPK_gen_1 440 448 PF00069 0.526
DOC_MAPK_MEF2A_6 683 692 PF00069 0.476
DOC_MAPK_RevD_3 216 231 PF00069 0.513
DOC_PP1_RVXF_1 454 461 PF00149 0.375
DOC_PP1_RVXF_1 613 620 PF00149 0.372
DOC_PP2B_LxvP_1 217 220 PF13499 0.406
DOC_PP4_FxxP_1 865 868 PF00568 0.573
DOC_USP7_MATH_1 130 134 PF00917 0.646
DOC_USP7_MATH_1 16 20 PF00917 0.568
DOC_USP7_MATH_1 237 241 PF00917 0.626
DOC_USP7_MATH_1 365 369 PF00917 0.560
DOC_USP7_MATH_1 380 384 PF00917 0.730
DOC_USP7_MATH_1 385 389 PF00917 0.677
DOC_USP7_MATH_1 416 420 PF00917 0.704
DOC_USP7_MATH_1 429 433 PF00917 0.645
DOC_USP7_MATH_1 43 47 PF00917 0.530
DOC_USP7_MATH_1 546 550 PF00917 0.710
DOC_USP7_MATH_1 563 567 PF00917 0.487
DOC_USP7_MATH_1 577 581 PF00917 0.473
DOC_USP7_MATH_1 825 829 PF00917 0.515
DOC_WW_Pin1_4 126 131 PF00397 0.637
DOC_WW_Pin1_4 244 249 PF00397 0.600
DOC_WW_Pin1_4 27 32 PF00397 0.632
DOC_WW_Pin1_4 318 323 PF00397 0.482
DOC_WW_Pin1_4 378 383 PF00397 0.678
DOC_WW_Pin1_4 387 392 PF00397 0.622
DOC_WW_Pin1_4 406 411 PF00397 0.683
DOC_WW_Pin1_4 510 515 PF00397 0.682
DOC_WW_Pin1_4 542 547 PF00397 0.623
DOC_WW_Pin1_4 55 60 PF00397 0.591
DOC_WW_Pin1_4 763 768 PF00397 0.747
DOC_WW_Pin1_4 840 845 PF00397 0.421
LIG_14-3-3_CanoR_1 275 281 PF00244 0.513
LIG_14-3-3_CanoR_1 328 333 PF00244 0.432
LIG_14-3-3_CanoR_1 340 346 PF00244 0.469
LIG_14-3-3_CanoR_1 44 50 PF00244 0.590
LIG_14-3-3_CanoR_1 515 523 PF00244 0.612
LIG_14-3-3_CanoR_1 581 587 PF00244 0.491
LIG_14-3-3_CanoR_1 644 648 PF00244 0.545
LIG_14-3-3_CanoR_1 70 75 PF00244 0.565
LIG_14-3-3_CanoR_1 725 729 PF00244 0.539
LIG_14-3-3_CanoR_1 849 854 PF00244 0.412
LIG_Actin_WH2_2 312 329 PF00022 0.397
LIG_Actin_WH2_2 600 617 PF00022 0.366
LIG_Actin_WH2_2 688 706 PF00022 0.528
LIG_BIR_II_1 1 5 PF00653 0.446
LIG_BIR_III_2 693 697 PF00653 0.514
LIG_BRCT_BRCA1_1 248 252 PF00533 0.656
LIG_BRCT_BRCA1_1 382 386 PF00533 0.568
LIG_CSL_BTD_1 543 546 PF09270 0.538
LIG_deltaCOP1_diTrp_1 343 346 PF00928 0.453
LIG_EH_1 260 264 PF12763 0.456
LIG_FHA_1 120 126 PF00498 0.595
LIG_FHA_1 168 174 PF00498 0.555
LIG_FHA_1 176 182 PF00498 0.506
LIG_FHA_1 200 206 PF00498 0.426
LIG_FHA_1 253 259 PF00498 0.509
LIG_FHA_1 350 356 PF00498 0.465
LIG_FHA_1 412 418 PF00498 0.662
LIG_FHA_1 559 565 PF00498 0.737
LIG_FHA_1 625 631 PF00498 0.494
LIG_FHA_1 715 721 PF00498 0.469
LIG_FHA_1 747 753 PF00498 0.653
LIG_FHA_1 76 82 PF00498 0.571
LIG_FHA_1 94 100 PF00498 0.400
LIG_FHA_2 158 164 PF00498 0.612
LIG_FHA_2 472 478 PF00498 0.623
LIG_FHA_2 772 778 PF00498 0.635
LIG_FHA_2 850 856 PF00498 0.402
LIG_Integrin_RGD_1 640 642 PF01839 0.501
LIG_LIR_Gen_1 20 31 PF02991 0.629
LIG_LIR_Gen_1 311 319 PF02991 0.381
LIG_LIR_Gen_1 343 354 PF02991 0.380
LIG_LIR_Gen_1 805 814 PF02991 0.479
LIG_LIR_Gen_1 846 853 PF02991 0.431
LIG_LIR_Nem_3 190 195 PF02991 0.419
LIG_LIR_Nem_3 20 26 PF02991 0.627
LIG_LIR_Nem_3 311 315 PF02991 0.373
LIG_LIR_Nem_3 343 349 PF02991 0.526
LIG_LIR_Nem_3 534 539 PF02991 0.555
LIG_LIR_Nem_3 541 547 PF02991 0.532
LIG_LIR_Nem_3 599 603 PF02991 0.370
LIG_LIR_Nem_3 667 671 PF02991 0.407
LIG_LIR_Nem_3 805 809 PF02991 0.387
LIG_LIR_Nem_3 828 833 PF02991 0.574
LIG_LIR_Nem_3 846 850 PF02991 0.330
LIG_LYPXL_yS_3 600 603 PF13949 0.393
LIG_MYND_1 400 404 PF01753 0.612
LIG_Pex14_2 292 296 PF04695 0.362
LIG_Pex14_2 312 316 PF04695 0.246
LIG_SH2_NCK_1 363 367 PF00017 0.442
LIG_SH2_STAP1 309 313 PF00017 0.349
LIG_SH2_STAP1 476 480 PF00017 0.552
LIG_SH2_STAP1 731 735 PF00017 0.571
LIG_SH2_STAT5 23 26 PF00017 0.585
LIG_SH2_STAT5 609 612 PF00017 0.408
LIG_SH2_STAT5 731 734 PF00017 0.600
LIG_SH3_3 28 34 PF00018 0.566
LIG_SH3_3 401 407 PF00018 0.572
LIG_SH3_3 540 546 PF00018 0.588
LIG_SH3_3 595 601 PF00018 0.366
LIG_SH3_3 693 699 PF00018 0.437
LIG_SH3_3 764 770 PF00018 0.641
LIG_Sin3_3 495 502 PF02671 0.532
LIG_SUMO_SIM_anti_2 810 816 PF11976 0.404
LIG_SUMO_SIM_par_1 204 210 PF11976 0.383
LIG_SUMO_SIM_par_1 351 356 PF11976 0.470
LIG_SUMO_SIM_par_1 560 566 PF11976 0.565
LIG_SUMO_SIM_par_1 627 634 PF11976 0.415
LIG_SUMO_SIM_par_1 812 818 PF11976 0.436
LIG_SUMO_SIM_par_1 90 96 PF11976 0.430
LIG_TRAF2_1 435 438 PF00917 0.546
LIG_TRAF2_1 588 591 PF00917 0.409
LIG_TRAF2_1 59 62 PF00917 0.539
LIG_TRAF2_1 653 656 PF00917 0.522
LIG_TYR_ITIM 598 603 PF00017 0.387
LIG_WRC_WIRS_1 315 320 PF05994 0.375
MOD_CDK_SPK_2 510 515 PF00069 0.581
MOD_CK1_1 126 132 PF00069 0.619
MOD_CK1_1 169 175 PF00069 0.551
MOD_CK1_1 247 253 PF00069 0.541
MOD_CK1_1 27 33 PF00069 0.607
MOD_CK1_1 381 387 PF00069 0.627
MOD_CK1_1 432 438 PF00069 0.635
MOD_CK1_1 485 491 PF00069 0.642
MOD_CK1_1 52 58 PF00069 0.599
MOD_CK1_1 580 586 PF00069 0.506
MOD_CK1_1 599 605 PF00069 0.362
MOD_CK1_1 73 79 PF00069 0.695
MOD_CK1_1 766 772 PF00069 0.636
MOD_CK2_1 157 163 PF00069 0.622
MOD_CK2_1 339 345 PF00069 0.361
MOD_CK2_1 432 438 PF00069 0.621
MOD_CK2_1 55 61 PF00069 0.585
MOD_CK2_1 563 569 PF00069 0.504
MOD_CK2_1 73 79 PF00069 0.648
MOD_CK2_1 780 786 PF00069 0.580
MOD_CK2_1 820 826 PF00069 0.460
MOD_CK2_1 840 846 PF00069 0.292
MOD_CK2_1 849 855 PF00069 0.436
MOD_CMANNOS 529 532 PF00535 0.591
MOD_Cter_Amidation 371 374 PF01082 0.549
MOD_GlcNHglycan 10 13 PF01048 0.494
MOD_GlcNHglycan 132 135 PF01048 0.567
MOD_GlcNHglycan 144 148 PF01048 0.572
MOD_GlcNHglycan 233 236 PF01048 0.664
MOD_GlcNHglycan 239 242 PF01048 0.625
MOD_GlcNHglycan 252 255 PF01048 0.462
MOD_GlcNHglycan 26 29 PF01048 0.592
MOD_GlcNHglycan 336 340 PF01048 0.352
MOD_GlcNHglycan 367 370 PF01048 0.718
MOD_GlcNHglycan 383 386 PF01048 0.580
MOD_GlcNHglycan 387 390 PF01048 0.633
MOD_GlcNHglycan 418 421 PF01048 0.760
MOD_GlcNHglycan 45 48 PF01048 0.757
MOD_GlcNHglycan 467 470 PF01048 0.535
MOD_GlcNHglycan 500 503 PF01048 0.607
MOD_GlcNHglycan 51 54 PF01048 0.615
MOD_GSK3_1 119 126 PF00069 0.599
MOD_GSK3_1 162 169 PF00069 0.577
MOD_GSK3_1 231 238 PF00069 0.672
MOD_GSK3_1 244 251 PF00069 0.536
MOD_GSK3_1 252 259 PF00069 0.673
MOD_GSK3_1 271 278 PF00069 0.461
MOD_GSK3_1 314 321 PF00069 0.373
MOD_GSK3_1 335 342 PF00069 0.338
MOD_GSK3_1 381 388 PF00069 0.730
MOD_GSK3_1 428 435 PF00069 0.610
MOD_GSK3_1 45 52 PF00069 0.686
MOD_GSK3_1 482 489 PF00069 0.535
MOD_GSK3_1 538 545 PF00069 0.618
MOD_GSK3_1 573 580 PF00069 0.696
MOD_GSK3_1 624 631 PF00069 0.499
MOD_GSK3_1 66 73 PF00069 0.667
MOD_GSK3_1 746 753 PF00069 0.669
MOD_GSK3_1 75 82 PF00069 0.488
MOD_GSK3_1 836 843 PF00069 0.445
MOD_N-GLC_1 118 123 PF02516 0.625
MOD_N-GLC_1 503 508 PF02516 0.601
MOD_N-GLC_1 55 60 PF02516 0.543
MOD_NEK2_1 100 105 PF00069 0.491
MOD_NEK2_1 166 171 PF00069 0.586
MOD_NEK2_1 24 29 PF00069 0.492
MOD_NEK2_1 335 340 PF00069 0.530
MOD_NEK2_1 349 354 PF00069 0.459
MOD_NEK2_1 465 470 PF00069 0.445
MOD_NEK2_1 482 487 PF00069 0.517
MOD_NEK2_1 729 734 PF00069 0.590
MOD_NEK2_1 794 799 PF00069 0.483
MOD_NEK2_1 8 13 PF00069 0.614
MOD_NEK2_1 815 820 PF00069 0.404
MOD_NEK2_1 92 97 PF00069 0.520
MOD_NEK2_2 322 327 PF00069 0.389
MOD_NEK2_2 699 704 PF00069 0.493
MOD_NEK2_2 80 85 PF00069 0.446
MOD_NEK2_2 825 830 PF00069 0.444
MOD_OFUCOSY 550 555 PF10250 0.656
MOD_PIKK_1 167 173 PF00454 0.577
MOD_PIKK_1 438 444 PF00454 0.511
MOD_PIKK_1 515 521 PF00454 0.616
MOD_PIKK_1 580 586 PF00454 0.489
MOD_PIKK_1 609 615 PF00454 0.372
MOD_PIKK_1 714 720 PF00454 0.544
MOD_PIKK_1 752 758 PF00454 0.694
MOD_PIKK_1 817 823 PF00454 0.426
MOD_PK_1 328 334 PF00069 0.445
MOD_PK_1 70 76 PF00069 0.562
MOD_PKA_2 229 235 PF00069 0.546
MOD_PKA_2 339 345 PF00069 0.515
MOD_PKA_2 421 427 PF00069 0.628
MOD_PKA_2 43 49 PF00069 0.636
MOD_PKA_2 432 438 PF00069 0.549
MOD_PKA_2 580 586 PF00069 0.510
MOD_PKA_2 643 649 PF00069 0.542
MOD_PKA_2 678 684 PF00069 0.464
MOD_PKA_2 724 730 PF00069 0.559
MOD_PKA_2 799 805 PF00069 0.409
MOD_Plk_1 162 168 PF00069 0.543
MOD_Plk_1 175 181 PF00069 0.531
MOD_Plk_1 256 262 PF00069 0.487
MOD_Plk_1 521 527 PF00069 0.483
MOD_Plk_1 590 596 PF00069 0.492
MOD_Plk_1 661 667 PF00069 0.509
MOD_Plk_1 699 705 PF00069 0.496
MOD_Plk_1 825 831 PF00069 0.483
MOD_Plk_2-3 157 163 PF00069 0.602
MOD_Plk_2-3 780 786 PF00069 0.600
MOD_Plk_4 169 175 PF00069 0.572
MOD_Plk_4 276 282 PF00069 0.470
MOD_Plk_4 349 355 PF00069 0.383
MOD_Plk_4 482 488 PF00069 0.546
MOD_Plk_4 590 596 PF00069 0.528
MOD_Plk_4 599 605 PF00069 0.413
MOD_Plk_4 661 667 PF00069 0.381
MOD_Plk_4 724 730 PF00069 0.501
MOD_Plk_4 794 800 PF00069 0.476
MOD_Plk_4 80 86 PF00069 0.548
MOD_ProDKin_1 126 132 PF00069 0.636
MOD_ProDKin_1 244 250 PF00069 0.599
MOD_ProDKin_1 27 33 PF00069 0.631
MOD_ProDKin_1 318 324 PF00069 0.487
MOD_ProDKin_1 378 384 PF00069 0.677
MOD_ProDKin_1 387 393 PF00069 0.622
MOD_ProDKin_1 406 412 PF00069 0.683
MOD_ProDKin_1 510 516 PF00069 0.679
MOD_ProDKin_1 542 548 PF00069 0.623
MOD_ProDKin_1 55 61 PF00069 0.588
MOD_ProDKin_1 763 769 PF00069 0.747
MOD_ProDKin_1 840 846 PF00069 0.421
MOD_SUMO_for_1 647 650 PF00179 0.671
MOD_SUMO_rev_2 473 481 PF00179 0.542
MOD_SUMO_rev_2 777 784 PF00179 0.656
TRG_DiLeu_BaEn_1 345 350 PF01217 0.368
TRG_DiLeu_BaLyEn_6 454 459 PF01217 0.385
TRG_DiLeu_BaLyEn_6 634 639 PF01217 0.485
TRG_ENDOCYTIC_2 23 26 PF00928 0.661
TRG_ENDOCYTIC_2 309 312 PF00928 0.350
TRG_ENDOCYTIC_2 600 603 PF00928 0.366
TRG_ENDOCYTIC_2 671 674 PF00928 0.380
TRG_ER_diArg_1 229 231 PF00400 0.615
TRG_ER_diArg_1 636 638 PF00400 0.463
TRG_ER_diArg_1 643 645 PF00400 0.452
TRG_NES_CRM1_1 324 337 PF08389 0.421
TRG_Pf-PMV_PEXEL_1 637 642 PF00026 0.518
TRG_Pf-PMV_PEXEL_1 831 835 PF00026 0.425
TRG_Pf-PMV_PEXEL_1 97 101 PF00026 0.595

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N0P6M5 Leptomonas seymouri 38% 100%
A0A3S7WX62 Leishmania donovani 99% 100%
A4HCE3 Leishmania braziliensis 63% 97%
E9AVS4 Leishmania mexicana (strain MHOM/GT/2001/U1103) 78% 97%
Q4QBQ5 Leishmania major 89% 100%

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS