LeishMANIAdb
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AAA domain-containing protein

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

Quick info

Protein:
AAA domain-containing protein
Gene product:
AAA ATPase domain containing protein - putative
Species:
Leishmania infantum
UniProt:
A4I2E8_LEIIN
TriTrypDb:
LINF_260027500
Length:
886

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: 0, no: 6
NetGPI no yes: 0, no: 6
Cellular components
Term Name Level Count
GO:0005634 nucleus 5 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0043229 intracellular organelle 3 1
GO:0043231 intracellular membrane-bounded organelle 4 1
GO:0110165 cellular anatomical entity 1 1

Expansion

Sequence features

A4I2E8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4I2E8

Function

Biological processes
Term Name Level Count
GO:0000075 cell cycle checkpoint signaling 4 1
GO:0000076 DNA replication checkpoint signaling 6 1
GO:0007093 mitotic cell cycle checkpoint signaling 4 1
GO:0007165 signal transduction 2 1
GO:0007346 regulation of mitotic cell cycle 5 1
GO:0009987 cellular process 1 1
GO:0010389 regulation of G2/M transition of mitotic cell cycle 7 1
GO:0010564 regulation of cell cycle process 5 1
GO:0010948 negative regulation of cell cycle process 6 1
GO:0010972 negative regulation of G2/M transition of mitotic cell cycle 8 1
GO:0022402 cell cycle process 2 1
GO:0031570 DNA integrity checkpoint signaling 5 1
GO:0033314 mitotic DNA replication checkpoint signaling 6 1
GO:0035556 intracellular signal transduction 3 1
GO:0044774 mitotic DNA integrity checkpoint signaling 5 1
GO:0044818 mitotic G2/M transition checkpoint 5 1
GO:0045786 negative regulation of cell cycle 5 1
GO:0045930 negative regulation of mitotic cell cycle 6 1
GO:0048519 negative regulation of biological process 3 1
GO:0048523 negative regulation of cellular process 4 1
GO:0050789 regulation of biological process 2 1
GO:0050794 regulation of cellular process 3 1
GO:0051726 regulation of cell cycle 4 1
GO:0065007 biological regulation 1 1
GO:1901987 regulation of cell cycle phase transition 6 1
GO:1901988 negative regulation of cell cycle phase transition 7 1
GO:1901990 regulation of mitotic cell cycle phase transition 6 1
GO:1901991 negative regulation of mitotic cell cycle phase transition 7 1
GO:1902749 regulation of cell cycle G2/M phase transition 7 1
GO:1902750 negative regulation of cell cycle G2/M phase transition 8 1
GO:1903047 mitotic cell cycle process 3 1
Molecular functions
Term Name Level Count
GO:0003676 nucleic acid binding 3 1
GO:0003677 DNA binding 4 1
GO:0003688 DNA replication origin binding 7 1
GO:0003690 double-stranded DNA binding 5 1
GO:0005488 binding 1 1
GO:0043565 sequence-specific DNA binding 5 1
GO:0097159 organic cyclic compound binding 2 1
GO:1901363 heterocyclic compound binding 2 1
GO:1990837 sequence-specific double-stranded DNA binding 6 1

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 367 371 PF00656 0.534
CLV_C14_Caspase3-7 39 43 PF00656 0.591
CLV_C14_Caspase3-7 658 662 PF00656 0.603
CLV_NRD_NRD_1 13 15 PF00675 0.709
CLV_NRD_NRD_1 147 149 PF00675 0.681
CLV_NRD_NRD_1 271 273 PF00675 0.648
CLV_NRD_NRD_1 29 31 PF00675 0.562
CLV_NRD_NRD_1 412 414 PF00675 0.583
CLV_NRD_NRD_1 524 526 PF00675 0.726
CLV_NRD_NRD_1 555 557 PF00675 0.396
CLV_NRD_NRD_1 72 74 PF00675 0.398
CLV_NRD_NRD_1 745 747 PF00675 0.413
CLV_PCSK_FUR_1 11 15 PF00082 0.654
CLV_PCSK_FUR_1 250 254 PF00082 0.578
CLV_PCSK_KEX2_1 13 15 PF00082 0.709
CLV_PCSK_KEX2_1 147 149 PF00082 0.583
CLV_PCSK_KEX2_1 252 254 PF00082 0.613
CLV_PCSK_KEX2_1 29 31 PF00082 0.562
CLV_PCSK_KEX2_1 411 413 PF00082 0.605
CLV_PCSK_KEX2_1 72 74 PF00082 0.398
CLV_PCSK_KEX2_1 747 749 PF00082 0.378
CLV_PCSK_KEX2_1 852 854 PF00082 0.446
CLV_PCSK_KEX2_1 97 99 PF00082 0.400
CLV_PCSK_PC1ET2_1 252 254 PF00082 0.615
CLV_PCSK_PC1ET2_1 411 413 PF00082 0.605
CLV_PCSK_PC1ET2_1 747 749 PF00082 0.378
CLV_PCSK_PC1ET2_1 852 854 PF00082 0.446
CLV_PCSK_PC1ET2_1 97 99 PF00082 0.400
CLV_PCSK_SKI1_1 150 154 PF00082 0.673
CLV_PCSK_SKI1_1 219 223 PF00082 0.654
CLV_PCSK_SKI1_1 272 276 PF00082 0.646
CLV_PCSK_SKI1_1 337 341 PF00082 0.455
CLV_PCSK_SKI1_1 436 440 PF00082 0.453
CLV_PCSK_SKI1_1 556 560 PF00082 0.405
CLV_PCSK_SKI1_1 97 101 PF00082 0.407
CLV_Separin_Metazoa 876 880 PF03568 0.457
DEG_SCF_FBW7_1 153 160 PF00400 0.636
DEG_SCF_FBW7_1 181 186 PF00400 0.683
DEG_SPOP_SBC_1 211 215 PF00917 0.552
DEG_SPOP_SBC_1 326 330 PF00917 0.605
DEG_SPOP_SBC_1 403 407 PF00917 0.639
DEG_SPOP_SBC_1 599 603 PF00917 0.580
DEG_SPOP_SBC_1 692 696 PF00917 0.559
DOC_CKS1_1 154 159 PF01111 0.612
DOC_CYCLIN_RxL_1 147 158 PF00134 0.665
DOC_CYCLIN_RxL_1 554 563 PF00134 0.405
DOC_MAPK_DCC_7 411 421 PF00069 0.539
DOC_MAPK_gen_1 537 546 PF00069 0.495
DOC_MAPK_gen_1 556 562 PF00069 0.339
DOC_MAPK_MEF2A_6 412 421 PF00069 0.529
DOC_MAPK_MEF2A_6 777 786 PF00069 0.488
DOC_PP1_RVXF_1 797 803 PF00149 0.520
DOC_PP4_FxxP_1 446 449 PF00568 0.461
DOC_USP7_MATH_1 161 165 PF00917 0.625
DOC_USP7_MATH_1 183 187 PF00917 0.604
DOC_USP7_MATH_1 199 203 PF00917 0.618
DOC_USP7_MATH_1 221 225 PF00917 0.642
DOC_USP7_MATH_1 230 234 PF00917 0.577
DOC_USP7_MATH_1 324 328 PF00917 0.766
DOC_USP7_MATH_1 331 335 PF00917 0.613
DOC_USP7_MATH_1 347 351 PF00917 0.360
DOC_USP7_MATH_1 364 368 PF00917 0.426
DOC_USP7_MATH_1 386 390 PF00917 0.553
DOC_USP7_MATH_1 398 402 PF00917 0.575
DOC_USP7_MATH_1 514 518 PF00917 0.609
DOC_USP7_MATH_1 528 532 PF00917 0.611
DOC_USP7_MATH_1 599 603 PF00917 0.580
DOC_USP7_MATH_1 608 612 PF00917 0.601
DOC_USP7_MATH_1 646 650 PF00917 0.522
DOC_USP7_MATH_1 677 681 PF00917 0.618
DOC_USP7_MATH_1 68 72 PF00917 0.410
DOC_USP7_MATH_1 692 696 PF00917 0.602
DOC_USP7_MATH_1 754 758 PF00917 0.541
DOC_WW_Pin1_4 153 158 PF00397 0.633
DOC_WW_Pin1_4 171 176 PF00397 0.575
DOC_WW_Pin1_4 179 184 PF00397 0.596
DOC_WW_Pin1_4 19 24 PF00397 0.701
DOC_WW_Pin1_4 195 200 PF00397 0.584
DOC_WW_Pin1_4 243 248 PF00397 0.677
DOC_WW_Pin1_4 327 332 PF00397 0.637
DOC_WW_Pin1_4 412 417 PF00397 0.560
DOC_WW_Pin1_4 509 514 PF00397 0.566
DOC_WW_Pin1_4 6 11 PF00397 0.615
DOC_WW_Pin1_4 600 605 PF00397 0.634
DOC_WW_Pin1_4 695 700 PF00397 0.616
DOC_WW_Pin1_4 764 769 PF00397 0.670
LIG_14-3-3_CanoR_1 101 109 PF00244 0.447
LIG_14-3-3_CanoR_1 203 209 PF00244 0.705
LIG_14-3-3_CanoR_1 323 331 PF00244 0.556
LIG_14-3-3_CanoR_1 530 538 PF00244 0.620
LIG_14-3-3_CanoR_1 540 548 PF00244 0.408
LIG_14-3-3_CanoR_1 575 584 PF00244 0.409
LIG_14-3-3_CanoR_1 618 623 PF00244 0.564
LIG_14-3-3_CanoR_1 657 665 PF00244 0.684
LIG_14-3-3_CanoR_1 833 838 PF00244 0.414
LIG_14-3-3_CanoR_1 861 869 PF00244 0.565
LIG_Actin_WH2_2 415 433 PF00022 0.470
LIG_Actin_WH2_2 816 831 PF00022 0.451
LIG_APCC_ABBA_1 476 481 PF00400 0.409
LIG_BIR_III_2 111 115 PF00653 0.484
LIG_BIR_III_4 177 181 PF00653 0.625
LIG_BIR_III_4 661 665 PF00653 0.613
LIG_BRCT_BRCA1_1 648 652 PF00533 0.577
LIG_BRCT_BRCA1_1 669 673 PF00533 0.559
LIG_EH1_1 44 52 PF00400 0.537
LIG_FHA_1 236 242 PF00498 0.730
LIG_FHA_1 273 279 PF00498 0.664
LIG_FHA_1 371 377 PF00498 0.388
LIG_FHA_1 612 618 PF00498 0.614
LIG_FHA_1 7 13 PF00498 0.556
LIG_FHA_1 731 737 PF00498 0.372
LIG_FHA_1 779 785 PF00498 0.474
LIG_FHA_1 829 835 PF00498 0.472
LIG_FHA_1 838 844 PF00498 0.462
LIG_FHA_1 91 97 PF00498 0.385
LIG_FHA_2 120 126 PF00498 0.629
LIG_FHA_2 128 134 PF00498 0.560
LIG_FHA_2 195 201 PF00498 0.692
LIG_FHA_2 238 244 PF00498 0.686
LIG_FHA_2 277 283 PF00498 0.604
LIG_FHA_2 47 53 PF00498 0.502
LIG_FHA_2 490 496 PF00498 0.445
LIG_FHA_2 726 732 PF00498 0.407
LIG_LIR_Apic_2 443 449 PF02991 0.349
LIG_LIR_Apic_2 840 844 PF02991 0.507
LIG_LIR_Gen_1 60 70 PF02991 0.405
LIG_LIR_Gen_1 871 882 PF02991 0.508
LIG_LIR_Nem_3 310 316 PF02991 0.428
LIG_LIR_Nem_3 333 339 PF02991 0.482
LIG_LIR_Nem_3 578 584 PF02991 0.410
LIG_LIR_Nem_3 60 66 PF02991 0.415
LIG_LIR_Nem_3 630 636 PF02991 0.435
LIG_LIR_Nem_3 819 823 PF02991 0.458
LIG_LIR_Nem_3 871 877 PF02991 0.512
LIG_LYPXL_yS_3 313 316 PF13949 0.409
LIG_PCNA_PIPBox_1 786 795 PF02747 0.479
LIG_Pex14_2 336 340 PF04695 0.452
LIG_SH2_CRK 551 555 PF00017 0.371
LIG_SH2_CRK 793 797 PF00017 0.401
LIG_SH2_GRB2like 343 346 PF00017 0.371
LIG_SH2_NCK_1 304 308 PF00017 0.503
LIG_SH2_NCK_1 479 483 PF00017 0.435
LIG_SH2_SRC 551 554 PF00017 0.376
LIG_SH2_STAP1 304 308 PF00017 0.503
LIG_SH2_STAP1 551 555 PF00017 0.371
LIG_SH2_STAP1 63 67 PF00017 0.400
LIG_SH2_STAP1 793 797 PF00017 0.401
LIG_SH2_STAT5 308 311 PF00017 0.433
LIG_SH2_STAT5 343 346 PF00017 0.404
LIG_SH2_STAT5 429 432 PF00017 0.429
LIG_SH2_STAT5 553 556 PF00017 0.411
LIG_SH2_STAT5 735 738 PF00017 0.411
LIG_SH2_STAT5 793 796 PF00017 0.406
LIG_SH3_3 293 299 PF00018 0.571
LIG_SH3_3 346 352 PF00018 0.423
LIG_SH3_3 461 467 PF00018 0.419
LIG_SUMO_SIM_anti_2 738 744 PF11976 0.403
LIG_SUMO_SIM_par_1 350 356 PF11976 0.457
LIG_SUMO_SIM_par_1 420 426 PF11976 0.363
LIG_SUMO_SIM_par_1 738 744 PF11976 0.363
LIG_TRAF2_1 122 125 PF00917 0.656
LIG_TRAF2_1 168 171 PF00917 0.703
LIG_UBA3_1 376 385 PF00899 0.468
LIG_WW_3 295 299 PF00397 0.619
MOD_CDK_SPK_2 157 162 PF00069 0.617
MOD_CDK_SPK_2 6 11 PF00069 0.612
MOD_CDK_SPxxK_3 19 26 PF00069 0.598
MOD_CDK_SPxxK_3 243 250 PF00069 0.570
MOD_CDK_SPxxK_3 509 516 PF00069 0.569
MOD_CDK_SPxxK_3 6 13 PF00069 0.670
MOD_CK1_1 185 191 PF00069 0.615
MOD_CK1_1 19 25 PF00069 0.642
MOD_CK1_1 194 200 PF00069 0.605
MOD_CK1_1 202 208 PF00069 0.601
MOD_CK1_1 224 230 PF00069 0.622
MOD_CK1_1 231 237 PF00069 0.620
MOD_CK1_1 264 270 PF00069 0.636
MOD_CK1_1 28 34 PF00069 0.648
MOD_CK1_1 318 324 PF00069 0.708
MOD_CK1_1 327 333 PF00069 0.627
MOD_CK1_1 407 413 PF00069 0.635
MOD_CK1_1 611 617 PF00069 0.601
MOD_CK1_1 653 659 PF00069 0.624
MOD_CK1_1 680 686 PF00069 0.557
MOD_CK1_1 695 701 PF00069 0.643
MOD_CK1_1 75 81 PF00069 0.416
MOD_CK2_1 118 124 PF00069 0.563
MOD_CK2_1 127 133 PF00069 0.564
MOD_CK2_1 237 243 PF00069 0.647
MOD_CK2_1 276 282 PF00069 0.607
MOD_CK2_1 46 52 PF00069 0.496
MOD_CK2_1 489 495 PF00069 0.448
MOD_CK2_1 624 630 PF00069 0.492
MOD_CK2_1 725 731 PF00069 0.412
MOD_GlcNHglycan 103 106 PF01048 0.442
MOD_GlcNHglycan 18 21 PF01048 0.556
MOD_GlcNHglycan 185 188 PF01048 0.553
MOD_GlcNHglycan 204 207 PF01048 0.691
MOD_GlcNHglycan 216 219 PF01048 0.480
MOD_GlcNHglycan 266 269 PF01048 0.688
MOD_GlcNHglycan 282 285 PF01048 0.514
MOD_GlcNHglycan 3 6 PF01048 0.777
MOD_GlcNHglycan 30 33 PF01048 0.648
MOD_GlcNHglycan 318 321 PF01048 0.652
MOD_GlcNHglycan 348 352 PF01048 0.427
MOD_GlcNHglycan 370 373 PF01048 0.367
MOD_GlcNHglycan 394 397 PF01048 0.584
MOD_GlcNHglycan 406 409 PF01048 0.663
MOD_GlcNHglycan 531 534 PF01048 0.626
MOD_GlcNHglycan 561 565 PF01048 0.438
MOD_GlcNHglycan 577 580 PF01048 0.437
MOD_GlcNHglycan 652 655 PF01048 0.727
MOD_GlcNHglycan 673 676 PF01048 0.623
MOD_GlcNHglycan 700 703 PF01048 0.517
MOD_GSK3_1 139 146 PF00069 0.698
MOD_GSK3_1 153 160 PF00069 0.556
MOD_GSK3_1 179 186 PF00069 0.768
MOD_GSK3_1 191 198 PF00069 0.604
MOD_GSK3_1 201 208 PF00069 0.605
MOD_GSK3_1 21 28 PF00069 0.797
MOD_GSK3_1 210 217 PF00069 0.489
MOD_GSK3_1 221 228 PF00069 0.551
MOD_GSK3_1 230 237 PF00069 0.670
MOD_GSK3_1 272 279 PF00069 0.666
MOD_GSK3_1 315 322 PF00069 0.585
MOD_GSK3_1 326 333 PF00069 0.557
MOD_GSK3_1 358 365 PF00069 0.403
MOD_GSK3_1 366 373 PF00069 0.467
MOD_GSK3_1 398 405 PF00069 0.677
MOD_GSK3_1 524 531 PF00069 0.620
MOD_GSK3_1 595 602 PF00069 0.614
MOD_GSK3_1 646 653 PF00069 0.697
MOD_GSK3_1 667 674 PF00069 0.545
MOD_GSK3_1 68 75 PF00069 0.402
MOD_GSK3_1 691 698 PF00069 0.581
MOD_GSK3_1 702 709 PF00069 0.474
MOD_GSK3_1 749 756 PF00069 0.487
MOD_GSK3_1 833 840 PF00069 0.427
MOD_N-GLC_1 235 240 PF02516 0.646
MOD_N-GLC_1 618 623 PF02516 0.609
MOD_N-GLC_1 78 83 PF02516 0.457
MOD_N-GLC_1 837 842 PF02516 0.440
MOD_NEK2_1 193 198 PF00069 0.629
MOD_NEK2_1 316 321 PF00069 0.451
MOD_NEK2_1 652 657 PF00069 0.581
MOD_NEK2_1 706 711 PF00069 0.453
MOD_NEK2_1 837 842 PF00069 0.442
MOD_NEK2_2 307 312 PF00069 0.467
MOD_NEK2_2 730 735 PF00069 0.392
MOD_NEK2_2 780 785 PF00069 0.457
MOD_OFUCOSY 359 366 PF10250 0.400
MOD_PIKK_1 21 27 PF00454 0.667
MOD_PIKK_1 331 337 PF00454 0.558
MOD_PIKK_1 370 376 PF00454 0.470
MOD_PK_1 36 42 PF00069 0.546
MOD_PK_1 618 624 PF00069 0.552
MOD_PKA_1 272 278 PF00069 0.611
MOD_PKA_1 72 78 PF00069 0.419
MOD_PKA_2 146 152 PF00069 0.693
MOD_PKA_2 161 167 PF00069 0.595
MOD_PKA_2 202 208 PF00069 0.689
MOD_PKA_2 228 234 PF00069 0.622
MOD_PKA_2 25 31 PF00069 0.723
MOD_PKA_2 322 328 PF00069 0.618
MOD_PKA_2 362 368 PF00069 0.467
MOD_PKA_2 507 513 PF00069 0.604
MOD_PKA_2 524 530 PF00069 0.652
MOD_PKA_2 539 545 PF00069 0.398
MOD_PKA_2 608 614 PF00069 0.577
MOD_PKA_2 656 662 PF00069 0.661
MOD_PKA_2 671 677 PF00069 0.514
MOD_PKA_2 72 78 PF00069 0.482
MOD_PKA_2 828 834 PF00069 0.454
MOD_PKA_2 860 866 PF00069 0.544
MOD_Plk_1 231 237 PF00069 0.648
MOD_Plk_1 618 624 PF00069 0.579
MOD_Plk_1 730 736 PF00069 0.385
MOD_Plk_1 749 755 PF00069 0.491
MOD_Plk_1 78 84 PF00069 0.455
MOD_Plk_2-3 634 640 PF00069 0.475
MOD_Plk_4 237 243 PF00069 0.612
MOD_Plk_4 436 442 PF00069 0.398
MOD_Plk_4 46 52 PF00069 0.496
MOD_Plk_4 62 68 PF00069 0.401
MOD_Plk_4 730 736 PF00069 0.385
MOD_Plk_4 78 84 PF00069 0.337
MOD_ProDKin_1 153 159 PF00069 0.631
MOD_ProDKin_1 171 177 PF00069 0.576
MOD_ProDKin_1 179 185 PF00069 0.593
MOD_ProDKin_1 19 25 PF00069 0.703
MOD_ProDKin_1 195 201 PF00069 0.585
MOD_ProDKin_1 243 249 PF00069 0.676
MOD_ProDKin_1 327 333 PF00069 0.634
MOD_ProDKin_1 412 418 PF00069 0.544
MOD_ProDKin_1 509 515 PF00069 0.567
MOD_ProDKin_1 6 12 PF00069 0.615
MOD_ProDKin_1 600 606 PF00069 0.639
MOD_ProDKin_1 695 701 PF00069 0.609
MOD_ProDKin_1 764 770 PF00069 0.672
MOD_SUMO_rev_2 267 275 PF00179 0.545
MOD_SUMO_rev_2 531 539 PF00179 0.597
TRG_DiLeu_BaEn_1 880 885 PF01217 0.493
TRG_DiLeu_BaLyEn_6 349 354 PF01217 0.381
TRG_DiLeu_BaLyEn_6 470 475 PF01217 0.406
TRG_ENDOCYTIC_2 308 311 PF00928 0.453
TRG_ENDOCYTIC_2 313 316 PF00928 0.387
TRG_ENDOCYTIC_2 551 554 PF00928 0.376
TRG_ENDOCYTIC_2 63 66 PF00928 0.404
TRG_ENDOCYTIC_2 793 796 PF00928 0.445
TRG_ER_diArg_1 10 13 PF00400 0.656
TRG_ER_diArg_1 147 150 PF00400 0.574
TRG_ER_diArg_1 546 549 PF00400 0.380
TRG_ER_diArg_1 72 74 PF00400 0.398
TRG_ER_diArg_1 745 748 PF00400 0.367
TRG_NLS_MonoExtN_4 250 256 PF00514 0.627
TRG_Pf-PMV_PEXEL_1 106 111 PF00026 0.468
TRG_Pf-PMV_PEXEL_1 165 170 PF00026 0.658
TRG_Pf-PMV_PEXEL_1 557 561 PF00026 0.410
TRG_Pf-PMV_PEXEL_1 72 77 PF00026 0.425

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1IIL4 Leptomonas seymouri 54% 100%
A0A3S7X053 Leishmania donovani 99% 100%
A4HF65 Leishmania braziliensis 76% 100%
E9AYK1 Leishmania mexicana (strain MHOM/GT/2001/U1103) 90% 100%
Q4Q8X1 Leishmania major 91% 98%

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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