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: E9AYC6
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 | 193 | 197 | PF00656 | 0.571 |
CLV_C14_Caspase3-7 | 452 | 456 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 485 | 489 | PF00656 | 0.338 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.233 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 265 | 267 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.469 |
CLV_PCSK_PC7_1 | 261 | 267 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.551 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.547 |
DEG_SPOP_SBC_1 | 45 | 49 | PF00917 | 0.623 |
DEG_SPOP_SBC_1 | 50 | 54 | PF00917 | 0.613 |
DOC_CYCLIN_RxL_1 | 261 | 270 | PF00134 | 0.360 |
DOC_CYCLIN_yCln2_LP_2 | 202 | 205 | PF00134 | 0.634 |
DOC_CYCLIN_yCln2_LP_2 | 78 | 84 | PF00134 | 0.430 |
DOC_MAPK_gen_1 | 265 | 271 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 461 | 471 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 88 | 97 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 323 | 330 | PF00069 | 0.450 |
DOC_MAPK_NFAT4_5 | 323 | 331 | PF00069 | 0.229 |
DOC_PP2B_LxvP_1 | 202 | 205 | PF13499 | 0.507 |
DOC_PP2B_LxvP_1 | 671 | 674 | PF13499 | 0.565 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 679 | 683 | PF00917 | 0.485 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.509 |
LIG_14-3-3_CanoR_1 | 14 | 21 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 266 | 272 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 289 | 293 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 627 | 637 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 698 | 706 | PF00244 | 0.423 |
LIG_Actin_WH2_2 | 501 | 518 | PF00022 | 0.508 |
LIG_BIR_III_4 | 441 | 445 | PF00653 | 0.468 |
LIG_Clathr_ClatBox_1 | 18 | 22 | PF01394 | 0.516 |
LIG_Clathr_ClatBox_1 | 300 | 304 | PF01394 | 0.363 |
LIG_deltaCOP1_diTrp_1 | 559 | 567 | PF00928 | 0.456 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.475 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.771 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.491 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.470 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.513 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.379 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.316 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.392 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.530 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.535 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.537 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.535 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.433 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.483 |
LIG_GBD_Chelix_1 | 146 | 154 | PF00786 | 0.373 |
LIG_Integrin_isoDGR_2 | 397 | 399 | PF01839 | 0.231 |
LIG_LIR_Gen_1 | 426 | 437 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 505 | 510 | PF02991 | 0.351 |
LIG_NRBOX | 363 | 369 | PF00104 | 0.474 |
LIG_PCNA_yPIPBox_3 | 361 | 371 | PF02747 | 0.456 |
LIG_PCNA_yPIPBox_3 | 378 | 388 | PF02747 | 0.478 |
LIG_PCNA_yPIPBox_3 | 579 | 588 | PF02747 | 0.498 |
LIG_PTB_Apo_2 | 686 | 693 | PF02174 | 0.266 |
LIG_SH2_GRB2like | 576 | 579 | PF00017 | 0.325 |
LIG_SH2_NCK_1 | 569 | 573 | PF00017 | 0.549 |
LIG_SH2_SRC | 250 | 253 | PF00017 | 0.434 |
LIG_SH2_SRC | 569 | 572 | PF00017 | 0.547 |
LIG_SH2_SRC | 650 | 653 | PF00017 | 0.523 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.424 |
LIG_SH2_STAT3 | 576 | 579 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 641 | 644 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 650 | 653 | PF00017 | 0.437 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.483 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.654 |
LIG_SUMO_SIM_anti_2 | 16 | 22 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 324 | 329 | PF11976 | 0.225 |
LIG_SUMO_SIM_anti_2 | 467 | 472 | PF11976 | 0.387 |
LIG_SUMO_SIM_anti_2 | 499 | 505 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 16 | 22 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 324 | 329 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 467 | 472 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 6 | 11 | PF11976 | 0.589 |
LIG_SUMO_SIM_par_1 | 669 | 677 | PF11976 | 0.445 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.411 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.349 |
LIG_UBA3_1 | 367 | 371 | PF00899 | 0.498 |
MOD_CDC14_SPxK_1 | 458 | 461 | PF00782 | 0.385 |
MOD_CDK_SPxK_1 | 455 | 461 | PF00069 | 0.405 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.442 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.729 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.727 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.431 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.745 |
MOD_CK1_1 | 672 | 678 | PF00069 | 0.404 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.729 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.339 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.686 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.398 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.535 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.445 |
MOD_CK2_1 | 657 | 663 | PF00069 | 0.651 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.702 |
MOD_Cter_Amidation | 313 | 316 | PF01082 | 0.420 |
MOD_Cter_Amidation | 519 | 522 | PF01082 | 0.457 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.536 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.531 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.659 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.603 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.585 |
MOD_GlcNHglycan | 455 | 458 | PF01048 | 0.539 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.650 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.528 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.530 |
MOD_GlcNHglycan | 615 | 618 | PF01048 | 0.231 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.664 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.652 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.459 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.739 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.427 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.580 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.218 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.506 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.698 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.521 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.716 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.552 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.656 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.709 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.402 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.430 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.738 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.397 |
MOD_N-GLC_1 | 657 | 662 | PF02516 | 0.658 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.595 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.399 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.616 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.435 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.330 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.449 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.613 |
MOD_NEK2_1 | 646 | 651 | PF00069 | 0.527 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.424 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.397 |
MOD_NEK2_2 | 267 | 272 | PF00069 | 0.456 |
MOD_NEK2_2 | 608 | 613 | PF00069 | 0.474 |
MOD_OFUCOSY | 153 | 160 | PF10250 | 0.383 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.442 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.482 |
MOD_PK_1 | 704 | 710 | PF00069 | 0.383 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.483 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.551 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.495 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.431 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.615 |
MOD_PKA_2 | 685 | 691 | PF00069 | 0.364 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.401 |
MOD_Plk_2-3 | 305 | 311 | PF00069 | 0.550 |
MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.519 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.471 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.531 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.574 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.390 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.449 |
MOD_Plk_4 | 637 | 643 | PF00069 | 0.461 |
MOD_Plk_4 | 679 | 685 | PF00069 | 0.569 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.614 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.397 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.522 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.498 |
MOD_SUMO_rev_2 | 174 | 184 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 517 | 523 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_1 | 594 | 599 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 463 | 466 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 561 | 564 | PF00400 | 0.600 |
TRG_NES_CRM1_1 | 500 | 512 | PF08389 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 388 | 393 | PF00026 | 0.265 |
TRG_Pf-PMV_PEXEL_1 | 580 | 584 | PF00026 | 0.298 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA19 | Leptomonas seymouri | 57% | 100% |
A0A0S4KLG2 | Bodo saltans | 36% | 100% |
A0A1X0NSS5 | Trypanosomatidae | 38% | 100% |
A0A3S7WZW4 | Leishmania donovani | 89% | 98% |
A0A422NJ04 | Trypanosoma rangeli | 39% | 100% |
A4HF02 | Leishmania braziliensis | 80% | 100% |
A4I281 | Leishmania infantum | 90% | 98% |
C9ZRR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
Q8WR00 | Leishmania major | 87% | 100% |
V5DA92 | Trypanosoma cruzi | 40% | 100% |