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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HBL0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006265 | DNA topological change | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0051276 | chromosome organization | 5 | 12 |
GO:0071103 | DNA conformation change | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003916 | DNA topoisomerase activity | 3 | 12 |
GO:0003917 | DNA topoisomerase type I (single strand cut, ATP-independent) activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.469 |
CLV_C14_Caspase3-7 | 724 | 728 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.219 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 747 | 749 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 791 | 793 | PF00675 | 0.585 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.207 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.188 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.158 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 776 | 778 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 791 | 793 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 776 | 778 | PF00082 | 0.454 |
CLV_PCSK_PC7_1 | 379 | 385 | PF00082 | 0.280 |
CLV_PCSK_PC7_1 | 394 | 400 | PF00082 | 0.147 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 784 | 788 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.252 |
DEG_MDM2_SWIB_1 | 96 | 103 | PF02201 | 0.506 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.534 |
DOC_CDC14_PxL_1 | 719 | 727 | PF14671 | 0.379 |
DOC_CKS1_1 | 221 | 226 | PF01111 | 0.232 |
DOC_CYCLIN_RxL_1 | 378 | 390 | PF00134 | 0.324 |
DOC_CYCLIN_RxL_1 | 87 | 97 | PF00134 | 0.350 |
DOC_MAPK_gen_1 | 148 | 156 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 3 | 14 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 445 | 451 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 457 | 465 | PF00069 | 0.198 |
DOC_MAPK_gen_1 | 544 | 550 | PF00069 | 0.401 |
DOC_MAPK_HePTP_8 | 146 | 158 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 148 | 156 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 220 | 228 | PF00069 | 0.246 |
DOC_MAPK_MEF2A_6 | 445 | 453 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 457 | 465 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 559 | 566 | PF00069 | 0.280 |
DOC_PP1_RVXF_1 | 65 | 72 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.401 |
DOC_PP2B_LxvP_1 | 651 | 654 | PF13499 | 0.348 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.262 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.178 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.190 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 756 | 760 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 790 | 794 | PF00917 | 0.463 |
DOC_USP7_UBL2_3 | 784 | 788 | PF12436 | 0.697 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.242 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.246 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 700 | 705 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 758 | 763 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 262 | 269 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 445 | 450 | PF00244 | 0.246 |
LIG_14-3-3_CanoR_1 | 582 | 587 | PF00244 | 0.232 |
LIG_14-3-3_CanoR_1 | 620 | 624 | PF00244 | 0.302 |
LIG_14-3-3_CanoR_1 | 683 | 693 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 733 | 742 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 791 | 797 | PF00244 | 0.469 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.421 |
LIG_BRCT_BRCA1_1 | 489 | 493 | PF00533 | 0.379 |
LIG_Clathr_ClatBox_1 | 12 | 16 | PF01394 | 0.419 |
LIG_CSL_BTD_1 | 70 | 73 | PF09270 | 0.436 |
LIG_deltaCOP1_diTrp_1 | 36 | 39 | PF00928 | 0.401 |
LIG_deltaCOP1_diTrp_1 | 486 | 493 | PF00928 | 0.246 |
LIG_EH1_1 | 321 | 329 | PF00400 | 0.324 |
LIG_EVH1_2 | 318 | 322 | PF00568 | 0.246 |
LIG_EVH1_2 | 562 | 566 | PF00568 | 0.280 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.421 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.232 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.247 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.339 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.356 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.276 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.408 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.246 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.354 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.452 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.296 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.506 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.268 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.457 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.461 |
LIG_Integrin_RGD_1 | 494 | 496 | PF01839 | 0.161 |
LIG_LIR_Gen_1 | 260 | 271 | PF02991 | 0.164 |
LIG_LIR_Gen_1 | 372 | 380 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 60 | 69 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 734 | 742 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.164 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 525 | 531 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 584 | 589 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 621 | 626 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 669 | 674 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 734 | 738 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.411 |
LIG_LYPXL_yS_3 | 586 | 589 | PF13949 | 0.232 |
LIG_PCNA_PIPBox_1 | 196 | 205 | PF02747 | 0.246 |
LIG_PCNA_PIPBox_1 | 739 | 748 | PF02747 | 0.331 |
LIG_PCNA_yPIPBox_3 | 106 | 116 | PF02747 | 0.424 |
LIG_PCNA_yPIPBox_3 | 144 | 153 | PF02747 | 0.421 |
LIG_PCNA_yPIPBox_3 | 733 | 746 | PF02747 | 0.338 |
LIG_Pex14_1 | 489 | 493 | PF04695 | 0.246 |
LIG_Pex14_2 | 631 | 635 | PF04695 | 0.232 |
LIG_Pex14_2 | 667 | 671 | PF04695 | 0.282 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.506 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.379 |
LIG_SH2_CRK | 374 | 378 | PF00017 | 0.246 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.264 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.264 |
LIG_SH2_GRB2like | 210 | 213 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 184 | 188 | PF00017 | 0.276 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.379 |
LIG_SH2_PTP2 | 598 | 601 | PF00017 | 0.232 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.379 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.280 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 674 | 677 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 745 | 748 | PF00017 | 0.363 |
LIG_SH3_1 | 559 | 565 | PF00018 | 0.247 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.401 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.291 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.322 |
LIG_SH3_3 | 430 | 436 | PF00018 | 0.379 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.238 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.124 |
LIG_SUMO_SIM_anti_2 | 10 | 17 | PF11976 | 0.250 |
LIG_SUMO_SIM_anti_2 | 284 | 290 | PF11976 | 0.161 |
LIG_SUMO_SIM_par_1 | 10 | 17 | PF11976 | 0.236 |
LIG_SUMO_SIM_par_1 | 225 | 231 | PF11976 | 0.232 |
LIG_SUMO_SIM_par_1 | 264 | 270 | PF11976 | 0.185 |
LIG_TRAF2_1 | 426 | 429 | PF00917 | 0.280 |
LIG_UBA3_1 | 146 | 153 | PF00899 | 0.385 |
LIG_UBA3_1 | 571 | 576 | PF00899 | 0.246 |
LIG_WRC_WIRS_1 | 664 | 669 | PF05994 | 0.286 |
LIG_WRC_WIRS_1 | 732 | 737 | PF05994 | 0.475 |
LIG_WRC_WIRS_1 | 93 | 98 | PF05994 | 0.506 |
LIG_WW_2 | 562 | 565 | PF00397 | 0.289 |
MOD_CDC14_SPxK_1 | 17 | 20 | PF00782 | 0.401 |
MOD_CDK_SPK_2 | 786 | 791 | PF00069 | 0.576 |
MOD_CDK_SPxK_1 | 14 | 20 | PF00069 | 0.401 |
MOD_CDK_SPxK_1 | 786 | 792 | PF00069 | 0.532 |
MOD_CDK_SPxxK_3 | 267 | 274 | PF00069 | 0.379 |
MOD_CDK_SPxxK_3 | 313 | 320 | PF00069 | 0.220 |
MOD_CDK_SPxxK_3 | 606 | 613 | PF00069 | 0.246 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.461 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.292 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.256 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.379 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.383 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.536 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.637 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.321 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.326 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.327 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.251 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.506 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.220 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.310 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.424 |
MOD_CK2_1 | 630 | 636 | PF00069 | 0.280 |
MOD_Cter_Amidation | 104 | 107 | PF01082 | 0.222 |
MOD_Cter_Amidation | 381 | 384 | PF01082 | 0.351 |
MOD_DYRK1A_RPxSP_1 | 220 | 224 | PF00069 | 0.232 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.338 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.266 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.413 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.381 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.449 |
MOD_GlcNHglycan | 696 | 700 | PF01048 | 0.407 |
MOD_GlcNHglycan | 752 | 755 | PF01048 | 0.562 |
MOD_GlcNHglycan | 762 | 765 | PF01048 | 0.532 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.443 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.343 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.167 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.462 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.243 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.519 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.189 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.232 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.302 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.320 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.205 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.247 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.286 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.387 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.472 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.486 |
MOD_GSK3_1 | 752 | 759 | PF00069 | 0.473 |
MOD_GSK3_1 | 765 | 772 | PF00069 | 0.598 |
MOD_GSK3_1 | 775 | 782 | PF00069 | 0.547 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.578 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.202 |
MOD_N-GLC_1 | 521 | 526 | PF02516 | 0.333 |
MOD_N-GLC_1 | 655 | 660 | PF02516 | 0.403 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.445 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.232 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.259 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.346 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.503 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.338 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.240 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.211 |
MOD_NEK2_1 | 738 | 743 | PF00069 | 0.442 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.436 |
MOD_NEK2_2 | 779 | 784 | PF00069 | 0.457 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.249 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.255 |
MOD_PKA_1 | 445 | 451 | PF00069 | 0.264 |
MOD_PKA_1 | 775 | 781 | PF00069 | 0.570 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.431 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.393 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.289 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.232 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.289 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.251 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.232 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.389 |
MOD_PKA_2 | 790 | 796 | PF00069 | 0.592 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.406 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.246 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.280 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.460 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.232 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.310 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.374 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.324 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.369 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.256 |
MOD_Plk_4 | 622 | 628 | PF00069 | 0.246 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.276 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.401 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.242 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.379 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.331 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.294 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.246 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.429 |
MOD_ProDKin_1 | 700 | 706 | PF00069 | 0.614 |
MOD_ProDKin_1 | 758 | 764 | PF00069 | 0.500 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.591 |
MOD_SUMO_for_1 | 22 | 25 | PF00179 | 0.411 |
MOD_SUMO_rev_2 | 113 | 120 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 230 | 236 | PF00179 | 0.247 |
MOD_SUMO_rev_2 | 25 | 34 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 524 | 531 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 633 | 639 | PF00179 | 0.294 |
TRG_DiLeu_BaLyEn_6 | 381 | 386 | PF01217 | 0.280 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.232 |
TRG_ENDOCYTIC_2 | 586 | 589 | PF00928 | 0.232 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.232 |
TRG_ENDOCYTIC_2 | 732 | 735 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 444 | 446 | PF00400 | 0.289 |
TRG_ER_diArg_1 | 746 | 748 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 790 | 792 | PF00400 | 0.652 |
TRG_Pf-PMV_PEXEL_1 | 106 | 110 | PF00026 | 0.211 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 438 | 442 | PF00026 | 0.259 |
TRG_Pf-PMV_PEXEL_1 | 613 | 617 | PF00026 | 0.324 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDE4 | Leptomonas seymouri | 68% | 93% |
A0A0S4JDQ6 | Bodo saltans | 39% | 98% |
A0A0S4JI21 | Bodo saltans | 22% | 82% |
A0A1X0NXB2 | Trypanosomatidae | 51% | 93% |
A0A3S7WW83 | Leishmania donovani | 85% | 99% |
A0A422N774 | Trypanosoma rangeli | 51% | 95% |
A0R5D9 | Mycolicibacterium smegmatis (strain ATCC 700084 / mc(2)155) | 27% | 85% |
A0R979 | Bacillus thuringiensis (strain Al Hakam) | 25% | 100% |
A4HZ99 | Leishmania infantum | 85% | 99% |
D0A1K4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 99% |
E9AUX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
O27661 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 24% | 100% |
O28469 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 27% | 100% |
O34204 | Fervidobacterium islandicum | 26% | 100% |
O51768 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 25% | 94% |
O58356 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 23% | 100% |
O67226 | Aquifex aeolicus (strain VF5) | 25% | 69% |
O69548 | Mycobacterium leprae (strain TN) | 27% | 84% |
O83409 | Treponema pallidum (strain Nichols) | 27% | 100% |
P06612 | Escherichia coli (strain K12) | 26% | 92% |
P0A2I1 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 26% | 92% |
P0A2I2 | Salmonella typhi | 26% | 92% |
P0A621 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 27% | 86% |
P0C2W6 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 21% | 100% |
P14294 | Escherichia coli (strain K12) | 21% | 100% |
P40687 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 22% | 100% |
P43012 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 25% | 92% |
P43704 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 21% | 100% |
P46799 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 24% | 100% |
P47368 | Mycoplasma genitalium (strain ATCC 33530 / DSM 19775 / NCTC 10195 / G37) | 25% | 100% |
P55991 | Helicobacter pylori (strain ATCC 700392 / 26695) | 26% | 100% |
P57371 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 24% | 93% |
P73810 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 29% | 89% |
P78032 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 25% | 100% |
P96583 | Bacillus subtilis (strain 168) | 25% | 100% |
P9WG48 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 27% | 86% |
P9WG49 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 27% | 86% |
Q06AK7 | Staphylococcus aureus | 25% | 100% |
Q1RIM1 | Rickettsia bellii (strain RML369-C) | 26% | 100% |
Q2FEN5 | Staphylococcus aureus (strain USA300) | 22% | 100% |
Q2FHI8 | Staphylococcus aureus (strain USA300) | 26% | 100% |
Q2FW03 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 22% | 100% |
Q2FZ32 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 26% | 100% |
Q2YXL8 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 25% | 100% |
Q49X35 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 25% | 100% |
Q4L5V2 | Staphylococcus haemolyticus (strain JCSC1435) | 26% | 100% |
Q4QCK3 | Leishmania major | 86% | 100% |
Q4UM42 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 25% | 100% |
Q59046 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 23% | 100% |
Q5HDV4 | Staphylococcus aureus (strain COL) | 22% | 100% |
Q5HGI2 | Staphylococcus aureus (strain COL) | 26% | 100% |
Q5HLZ4 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 22% | 100% |
Q5UQB5 | Acanthamoeba polyphaga mimivirus | 24% | 94% |
Q5WAX6 | Alkalihalobacillus clausii (strain KSM-K16) | 24% | 100% |
Q63GK5 | Bacillus cereus (strain ZK / E33L) | 25% | 100% |
Q65N90 | Bacillus licheniformis (strain ATCC 14580 / DSM 13 / JCM 2505 / CCUG 7422 / NBRC 12200 / NCIMB 9375 / NCTC 10341 / NRRL NRS-1264 / Gibson 46) | 25% | 100% |
Q68X45 | Rickettsia typhi (strain ATCC VR-144 / Wilmington) | 26% | 100% |
Q6G767 | Staphylococcus aureus (strain MSSA476) | 22% | 100% |
Q6G9W3 | Staphylococcus aureus (strain MSSA476) | 26% | 100% |
Q6GEH9 | Staphylococcus aureus (strain MRSA252) | 21% | 100% |
Q6GHI5 | Staphylococcus aureus (strain MRSA252) | 26% | 100% |
Q6HP19 | Bacillus thuringiensis subsp. konkukian (strain 97-27) | 25% | 100% |
Q73E74 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 25% | 100% |
Q7A075 | Staphylococcus aureus (strain MW2) | 22% | 100% |
Q7A455 | Staphylococcus aureus (strain N315) | 22% | 100% |
Q7A5Y5 | Staphylococcus aureus (strain N315) | 26% | 100% |
Q81IH1 | Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) | 26% | 100% |
Q81Z97 | Bacillus anthracis | 25% | 100% |
Q87AQ6 | Xylella fastidiosa (strain Temecula1 / ATCC 700964) | 27% | 98% |
Q8CRF7 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 22% | 100% |
Q8K9P7 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 24% | 94% |
Q8NWZ9 | Staphylococcus aureus (strain MW2) | 26% | 100% |
Q8Z6F5 | Salmonella typhi | 22% | 100% |
Q92IH1 | Rickettsia conorii (strain ATCC VR-613 / Malish 7) | 26% | 100% |
Q97ZF5 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 26% | 69% |
Q99S17 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 22% | 100% |
Q99UM1 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 26% | 100% |
Q9CN30 | Pasteurella multocida (strain Pm70) | 27% | 92% |
Q9CP53 | Pasteurella multocida (strain Pm70) | 22% | 100% |
Q9HM08 | Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) | 25% | 100% |
Q9HZJ5 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 26% | 92% |
Q9JN65 | Mycoplasma gallisepticum (strain R(low / passage 15 / clone 2)) | 24% | 100% |
Q9KA23 | Halalkalibacterium halodurans (strain ATCC BAA-125 / DSM 18197 / FERM 7344 / JCM 9153 / C-125) | 25% | 100% |
Q9KQF5 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 23% | 100% |
Q9KRB2 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 26% | 91% |
Q9PEV8 | Xylella fastidiosa (strain 9a5c) | 27% | 98% |
Q9PHK2 | Xylella fastidiosa (strain 9a5c) | 27% | 100% |
Q9PLZ2 | Campylobacter jejuni subsp. jejuni serotype O:2 (strain ATCC 700819 / NCTC 11168) | 27% | 100% |
Q9UYS8 | Pyrococcus abyssi (strain GE5 / Orsay) | 23% | 100% |
Q9X909 | Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) | 27% | 84% |
Q9YB01 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 22% | 100% |
Q9ZDK2 | Rickettsia prowazekii (strain Madrid E) | 25% | 100% |
Q9ZMV7 | Helicobacter pylori (strain J99 / ATCC 700824) | 27% | 100% |
V5BG04 | Trypanosoma cruzi | 52% | 97% |