A large and likely artifical grouping of protease domain carrying proteins related to proteasomal proteases. Only a tiny subgroup (the AFG3-related mitochondrail proteins) seem to have a TM segment.. Localization: Cytoplasmic (by homology) / Mitochondrial (by homology)
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:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005745 | m-AAA complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 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:1902494 | catalytic complex | 2 | 1 |
GO:1905368 | peptidase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HAL9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016485 | protein processing | 5 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0034982 | mitochondrial protein processing | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004175 | endopeptidase activity | 4 | 12 |
GO:0004176 | ATP-dependent peptidase activity | 2 | 12 |
GO:0004222 | metalloendopeptidase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008233 | peptidase activity | 3 | 12 |
GO:0008237 | metallopeptidase activity | 4 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.396 |
CLV_C14_Caspase3-7 | 486 | 490 | PF00656 | 0.396 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.197 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.195 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.196 |
CLV_PCSK_FUR_1 | 446 | 450 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.196 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 330 | 332 | PF00082 | 0.286 |
CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.196 |
CLV_PCSK_PC7_1 | 326 | 332 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.196 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.196 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.196 |
DEG_APCC_KENBOX_2 | 721 | 725 | PF00400 | 0.443 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.517 |
DEG_SCF_FBW7_1 | 170 | 177 | PF00400 | 0.524 |
DEG_SCF_FBW7_1 | 541 | 546 | PF00400 | 0.407 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.718 |
DOC_CDC14_PxL_1 | 288 | 296 | PF14671 | 0.196 |
DOC_CKS1_1 | 171 | 176 | PF01111 | 0.541 |
DOC_CKS1_1 | 96 | 101 | PF01111 | 0.553 |
DOC_CYCLIN_RxL_1 | 419 | 427 | PF00134 | 0.500 |
DOC_CYCLIN_yCln2_LP_2 | 714 | 720 | PF00134 | 0.500 |
DOC_MAPK_gen_1 | 200 | 210 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 494 | 504 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 510 | 517 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 510 | 517 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 722 | 730 | PF00069 | 0.465 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.745 |
DOC_USP7_UBL2_3 | 506 | 510 | PF12436 | 0.469 |
DOC_USP7_UBL2_3 | 587 | 591 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 180 | 185 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 200 | 206 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 222 | 230 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 28 | 37 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 314 | 319 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 326 | 330 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 500 | 505 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 632 | 640 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.602 |
LIG_BIR_III_4 | 442 | 446 | PF00653 | 0.407 |
LIG_BIR_III_4 | 472 | 476 | PF00653 | 0.407 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.579 |
LIG_BRCT_BRCA1_1 | 494 | 498 | PF00533 | 0.396 |
LIG_Clathr_ClatBox_1 | 582 | 586 | PF01394 | 0.487 |
LIG_CSL_BTD_1 | 289 | 292 | PF09270 | 0.207 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.597 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.632 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.587 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.396 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.396 |
LIG_FHA_1 | 750 | 756 | PF00498 | 0.433 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.699 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.701 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.224 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.443 |
LIG_FHA_2 | 784 | 790 | PF00498 | 0.556 |
LIG_HCF-1_HBM_1 | 747 | 750 | PF13415 | 0.341 |
LIG_Integrin_isoDGR_2 | 255 | 257 | PF01839 | 0.449 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.254 |
LIG_LIR_Gen_1 | 266 | 271 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 363 | 373 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 407 | 416 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 666 | 677 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 769 | 779 | PF02991 | 0.405 |
LIG_LIR_LC3C_4 | 4 | 9 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 204 | 208 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.219 |
LIG_LIR_Nem_3 | 363 | 368 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 666 | 672 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 769 | 774 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 781 | 787 | PF02991 | 0.483 |
LIG_LYPXL_yS_3 | 288 | 291 | PF13949 | 0.284 |
LIG_NRBOX | 210 | 216 | PF00104 | 0.376 |
LIG_PTB_Apo_2 | 303 | 310 | PF02174 | 0.509 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.545 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.268 |
LIG_SH2_CRK | 365 | 369 | PF00017 | 0.481 |
LIG_SH2_PTP2 | 413 | 416 | PF00017 | 0.407 |
LIG_SH2_SRC | 787 | 790 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.221 |
LIG_SH2_STAP1 | 3 | 7 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.481 |
LIG_SH2_STAT3 | 224 | 227 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 787 | 790 | PF00017 | 0.495 |
LIG_SH3_2 | 717 | 722 | PF14604 | 0.396 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.657 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.613 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.364 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.287 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.427 |
LIG_SH3_3 | 714 | 720 | PF00018 | 0.396 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.697 |
LIG_SH3_4 | 506 | 513 | PF00018 | 0.454 |
LIG_SUMO_SIM_anti_2 | 351 | 357 | PF11976 | 0.450 |
LIG_SUMO_SIM_anti_2 | 474 | 480 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 240 | 246 | PF11976 | 0.252 |
LIG_SUMO_SIM_par_1 | 351 | 357 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 6 | 11 | PF11976 | 0.579 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.529 |
LIG_TRAF2_1 | 646 | 649 | PF00917 | 0.421 |
LIG_TRFH_1 | 182 | 186 | PF08558 | 0.336 |
LIG_TYR_ITSM | 284 | 291 | PF00017 | 0.367 |
LIG_WRC_WIRS_1 | 267 | 272 | PF05994 | 0.454 |
MOD_CDC14_SPxK_1 | 128 | 131 | PF00782 | 0.617 |
MOD_CDK_SPxK_1 | 125 | 131 | PF00069 | 0.627 |
MOD_CDK_SPxK_1 | 77 | 83 | PF00069 | 0.472 |
MOD_CDK_SPxxK_3 | 125 | 132 | PF00069 | 0.522 |
MOD_CDK_SPxxK_3 | 182 | 189 | PF00069 | 0.416 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.467 |
MOD_CDK_SPxxK_3 | 590 | 597 | PF00069 | 0.376 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.289 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.436 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.322 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.610 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.235 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.554 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.376 |
MOD_CK1_1 | 736 | 742 | PF00069 | 0.279 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.541 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.711 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.414 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.402 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.231 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.265 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.265 |
MOD_CK2_1 | 783 | 789 | PF00069 | 0.501 |
MOD_Cter_Amidation | 444 | 447 | PF01082 | 0.231 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.325 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.298 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.435 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.649 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.246 |
MOD_GlcNHglycan | 472 | 476 | PF01048 | 0.325 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.231 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.263 |
MOD_GlcNHglycan | 586 | 590 | PF01048 | 0.433 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.567 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.259 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.426 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.488 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.296 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.415 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.547 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.231 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.241 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.528 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.237 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.462 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.157 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.376 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.376 |
MOD_GSK3_1 | 783 | 790 | PF00069 | 0.423 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.582 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.463 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.374 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.476 |
MOD_N-GLC_1 | 452 | 457 | PF02516 | 0.376 |
MOD_N-GLC_2 | 552 | 554 | PF02516 | 0.231 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.486 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.454 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.207 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.472 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.455 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.443 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.237 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.231 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.417 |
MOD_NEK2_1 | 749 | 754 | PF00069 | 0.290 |
MOD_NEK2_2 | 111 | 116 | PF00069 | 0.472 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.574 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.684 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.562 |
MOD_PIKK_1 | 633 | 639 | PF00454 | 0.231 |
MOD_PIKK_1 | 644 | 650 | PF00454 | 0.231 |
MOD_PK_1 | 331 | 337 | PF00069 | 0.366 |
MOD_PKA_1 | 447 | 453 | PF00069 | 0.231 |
MOD_PKA_1 | 500 | 506 | PF00069 | 0.231 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.500 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.231 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.231 |
MOD_PKB_1 | 628 | 636 | PF00069 | 0.265 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.474 |
MOD_Plk_1 | 23 | 29 | PF00069 | 0.455 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.331 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.386 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.451 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.353 |
MOD_Plk_1 | 585 | 591 | PF00069 | 0.419 |
MOD_Plk_1 | 710 | 716 | PF00069 | 0.261 |
MOD_Plk_2-3 | 266 | 272 | PF00069 | 0.441 |
MOD_Plk_2-3 | 505 | 511 | PF00069 | 0.389 |
MOD_Plk_2-3 | 783 | 789 | PF00069 | 0.415 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.367 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.360 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.231 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.244 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.151 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.711 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.331 |
MOD_Plk_4 | 783 | 789 | PF00069 | 0.384 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.594 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.548 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.562 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.362 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.246 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.728 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.376 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.595 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.559 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.501 |
MOD_SUMO_for_1 | 329 | 332 | PF00179 | 0.346 |
MOD_SUMO_for_1 | 348 | 351 | PF00179 | 0.307 |
MOD_SUMO_for_1 | 760 | 763 | PF00179 | 0.325 |
MOD_SUMO_rev_2 | 495 | 503 | PF00179 | 0.231 |
TRG_DiLeu_BaEn_1 | 277 | 282 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_2 | 253 | 259 | PF01217 | 0.346 |
TRG_DiLeu_BaEn_2 | 353 | 359 | PF01217 | 0.304 |
TRG_DiLeu_BaLyEn_6 | 647 | 652 | PF01217 | 0.376 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.246 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 627 | 630 | PF00400 | 0.265 |
TRG_NLS_MonoCore_2 | 445 | 450 | PF00514 | 0.231 |
TRG_NLS_MonoExtC_3 | 445 | 451 | PF00514 | 0.231 |
TRG_Pf-PMV_PEXEL_1 | 189 | 194 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 422 | 427 | PF00026 | 0.231 |
TRG_Pf-PMV_PEXEL_1 | 742 | 746 | PF00026 | 0.325 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6C1 | Leptomonas seymouri | 89% | 100% |
A0A0S4KHE9 | Bodo saltans | 55% | 98% |
A0A1X0P9F5 | Trypanosomatidae | 68% | 100% |
A0A3Q8IFG3 | Leishmania donovani | 35% | 100% |
A0A3Q8IHD0 | Leishmania donovani | 95% | 100% |
A0A3Q8IJP7 | Leishmania donovani | 38% | 100% |
A0A3S5H775 | Leishmania donovani | 36% | 100% |
A0A3S5H828 | Leishmania donovani | 40% | 100% |
A0A422N673 | Trypanosoma rangeli | 66% | 100% |
A0LN68 | Syntrophobacter fumaroxidans (strain DSM 10017 / MPOB) | 41% | 100% |
A0PXM8 | Clostridium novyi (strain NT) | 39% | 100% |
A4H9H1 | Leishmania braziliensis | 38% | 100% |
A4HAA8 | Leishmania braziliensis | 36% | 100% |
A4HPD5 | Leishmania braziliensis | 40% | 100% |
A4HXT7 | Leishmania infantum | 38% | 100% |
A4HYI8 | Leishmania infantum | 37% | 100% |
A4I809 | Leishmania infantum | 35% | 100% |
A4I9Q6 | Leishmania infantum | 95% | 100% |
A4ICH8 | Leishmania infantum | 40% | 100% |
A6LD25 | Parabacteroides distasonis (strain ATCC 8503 / DSM 20701 / CIP 104284 / JCM 5825 / NCTC 11152) | 41% | 100% |
A6TSZ1 | Alkaliphilus metalliredigens (strain QYMF) | 35% | 100% |
A8ZNZ4 | Acaryochloris marina (strain MBIC 11017) | 39% | 100% |
B0B970 | Chlamydia trachomatis serovar L2 (strain 434/Bu / ATCC VR-902B) | 37% | 87% |
C1F8X6 | Acidobacterium capsulatum (strain ATCC 51196 / DSM 11244 / BCRC 80197 / JCM 7670 / NBRC 15755 / NCIMB 13165 / 161) | 37% | 100% |
C7M0M0 | Acidimicrobium ferrooxidans (strain DSM 10331 / JCM 15462 / NBRC 103882 / ICP) | 39% | 100% |
C8WEG0 | Zymomonas mobilis subsp. mobilis (strain NCIMB 11163 / B70) | 39% | 100% |
C9ZMX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 67% | 100% |
D5HA94 | Salinibacter ruber (strain M8) | 38% | 100% |
E9ARJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9ASB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AT49 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9B2S6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B4S8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
P57462 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 37% | 100% |
P73179 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 38% | 100% |
Q3JMH0 | Burkholderia pseudomallei (strain 1710b) | 39% | 100% |
Q4Q1E9 | Leishmania major | 40% | 100% |
Q4Q399 | Leishmania major | 95% | 100% |
Q4Q5D1 | Leishmania major | 35% | 100% |
Q4QD50 | Leishmania major | 36% | 100% |
Q4QDY0 | Leishmania major | 38% | 100% |
Q6F0E5 | Mesoplasma florum (strain ATCC 33453 / NBRC 100688 / NCTC 11704 / L1) | 36% | 100% |
V5BEV9 | Trypanosoma cruzi | 68% | 100% |