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:0005965 | protein farnesyltransferase complex | 4 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1990234 | transferase complex | 3 | 12 |
Related structures:
AlphaFold database: A0A3S7WZW4
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0018342 | protein prenylation | 4 | 12 |
GO:0018343 | protein farnesylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0097354 | prenylation | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004659 | prenyltransferase activity | 4 | 12 |
GO:0004660 | protein farnesyltransferase activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008318 | protein prenyltransferase activity | 3 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0008270 | zinc ion binding | 6 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 206 | 210 | PF00656 | 0.739 |
CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.699 |
CLV_C14_Caspase3-7 | 644 | 648 | PF00656 | 0.576 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.278 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.635 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 534 | 536 | PF00082 | 0.596 |
CLV_PCSK_PC7_1 | 274 | 280 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.649 |
DEG_SPOP_SBC_1 | 46 | 50 | PF00917 | 0.750 |
DEG_SPOP_SBC_1 | 51 | 55 | PF00917 | 0.729 |
DEG_SPOP_SBC_1 | 687 | 691 | PF00917 | 0.381 |
DOC_CYCLIN_RxL_1 | 274 | 283 | PF00134 | 0.413 |
DOC_CYCLIN_yCln2_LP_2 | 81 | 87 | PF00134 | 0.500 |
DOC_MAPK_gen_1 | 228 | 236 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 278 | 284 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 474 | 484 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 91 | 100 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 336 | 343 | PF00069 | 0.549 |
DOC_PP2B_LxvP_1 | 684 | 687 | PF13499 | 0.640 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.409 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.657 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 302 | 306 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 535 | 545 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 640 | 650 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 699 | 703 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 711 | 719 | PF00244 | 0.472 |
LIG_Actin_WH2_2 | 514 | 531 | PF00022 | 0.649 |
LIG_BRCT_BRCA1_1 | 701 | 705 | PF00533 | 0.480 |
LIG_Clathr_ClatBox_1 | 19 | 23 | PF01394 | 0.558 |
LIG_Clathr_ClatBox_1 | 313 | 317 | PF01394 | 0.428 |
LIG_CSL_BTD_1 | 214 | 217 | PF09270 | 0.465 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.625 |
LIG_deltaCOP1_diTrp_1 | 572 | 580 | PF00928 | 0.666 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.485 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.772 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.763 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.535 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.483 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.545 |
LIG_FHA_1 | 699 | 705 | PF00498 | 0.443 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.602 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.519 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.562 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.790 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.562 |
LIG_FHA_2 | 642 | 648 | PF00498 | 0.650 |
LIG_FHA_2 | 651 | 657 | PF00498 | 0.537 |
LIG_FHA_2 | 689 | 695 | PF00498 | 0.461 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.568 |
LIG_GBD_Chelix_1 | 149 | 157 | PF00786 | 0.532 |
LIG_Integrin_isoDGR_2 | 410 | 412 | PF01839 | 0.276 |
LIG_LIR_Apic_2 | 212 | 218 | PF02991 | 0.586 |
LIG_LIR_Apic_2 | 86 | 90 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 439 | 446 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 539 | 550 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 190 | 194 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.613 |
LIG_NRBOX | 376 | 382 | PF00104 | 0.517 |
LIG_PCNA_yPIPBox_3 | 374 | 384 | PF02747 | 0.501 |
LIG_PCNA_yPIPBox_3 | 391 | 401 | PF02747 | 0.501 |
LIG_PCNA_yPIPBox_3 | 592 | 601 | PF02747 | 0.530 |
LIG_PDZ_Class_1 | 720 | 725 | PF00595 | 0.488 |
LIG_RPA_C_Fungi | 706 | 718 | PF08784 | 0.502 |
LIG_SH2_GRB2like | 589 | 592 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 582 | 586 | PF00017 | 0.609 |
LIG_SH2_SRC | 263 | 266 | PF00017 | 0.491 |
LIG_SH2_SRC | 582 | 585 | PF00017 | 0.618 |
LIG_SH2_SRC | 663 | 666 | PF00017 | 0.608 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 542 | 546 | PF00017 | 0.622 |
LIG_SH2_STAT3 | 589 | 592 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 654 | 657 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.522 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.524 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.513 |
LIG_SUMO_SIM_anti_2 | 17 | 23 | PF11976 | 0.470 |
LIG_SUMO_SIM_anti_2 | 480 | 485 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.538 |
LIG_SUMO_SIM_par_1 | 339 | 345 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 480 | 485 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 7 | 12 | PF11976 | 0.610 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.530 |
LIG_TYR_ITIM | 122 | 127 | PF00017 | 0.390 |
LIG_UBA3_1 | 380 | 384 | PF00899 | 0.413 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.417 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.748 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.773 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.344 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.654 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.757 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.769 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.328 |
MOD_CK1_1 | 669 | 675 | PF00069 | 0.760 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.752 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.448 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.518 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.449 |
MOD_CK2_1 | 650 | 656 | PF00069 | 0.534 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.703 |
MOD_CK2_1 | 688 | 694 | PF00069 | 0.522 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.728 |
MOD_Cter_Amidation | 326 | 329 | PF01082 | 0.590 |
MOD_Cter_Amidation | 532 | 535 | PF01082 | 0.569 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.553 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.567 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.643 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.763 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.709 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.644 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.785 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.605 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.615 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.328 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.720 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.700 |
MOD_GlcNHglycan | 713 | 716 | PF01048 | 0.474 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.759 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.590 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.224 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.462 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.731 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.717 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.415 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.503 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.748 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.579 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.747 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.456 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.474 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.734 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.509 |
MOD_N-GLC_1 | 687 | 692 | PF02516 | 0.571 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.703 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.467 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.761 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.503 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.328 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.666 |
MOD_NEK2_1 | 659 | 664 | PF00069 | 0.581 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.488 |
MOD_NEK2_2 | 111 | 116 | PF00069 | 0.509 |
MOD_NEK2_2 | 280 | 285 | PF00069 | 0.363 |
MOD_NEK2_2 | 621 | 626 | PF00069 | 0.385 |
MOD_OFUCOSY | 156 | 163 | PF10250 | 0.540 |
MOD_PIKK_1 | 370 | 376 | PF00454 | 0.344 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.522 |
MOD_PK_1 | 717 | 723 | PF00069 | 0.491 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.533 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.726 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.449 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.551 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.328 |
MOD_PKA_2 | 666 | 672 | PF00069 | 0.690 |
MOD_PKA_2 | 698 | 704 | PF00069 | 0.431 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.513 |
MOD_Plk_2-3 | 318 | 324 | PF00069 | 0.570 |
MOD_Plk_2-3 | 7 | 13 | PF00069 | 0.564 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.526 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.639 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.448 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.342 |
MOD_Plk_4 | 650 | 656 | PF00069 | 0.502 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.617 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.622 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.474 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.413 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.507 |
MOD_SUMO_rev_2 | 485 | 495 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 530 | 536 | PF00179 | 0.650 |
TRG_DiLeu_BaEn_1 | 607 | 612 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 541 | 546 | PF01217 | 0.609 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 542 | 545 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 582 | 585 | PF00928 | 0.618 |
TRG_ER_diArg_1 | 394 | 396 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.682 |
TRG_Pf-PMV_PEXEL_1 | 401 | 406 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 544 | 549 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 593 | 597 | PF00026 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA19 | Leptomonas seymouri | 57% | 100% |
A0A0S4KLG2 | Bodo saltans | 39% | 100% |
A0A1X0NSS5 | Trypanosomatidae | 37% | 100% |
A0A422NJ04 | Trypanosoma rangeli | 39% | 100% |
A4HF02 | Leishmania braziliensis | 81% | 100% |
A4I281 | Leishmania infantum | 99% | 100% |
C9ZRR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AYC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 98% |
Q8WR00 | Leishmania major | 93% | 100% |
V5DA92 | Trypanosoma cruzi | 39% | 100% |