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: A4HF02
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 | 226 | 230 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.323 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.645 |
CLV_C14_Caspase3-7 | 558 | 562 | PF00656 | 0.545 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.233 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.242 |
CLV_PCSK_PC7_1 | 276 | 282 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.635 |
CLV_Separin_Metazoa | 528 | 532 | PF03568 | 0.423 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.565 |
DEG_SPOP_SBC_1 | 178 | 182 | PF00917 | 0.388 |
DEG_SPOP_SBC_1 | 50 | 54 | PF00917 | 0.607 |
DEG_SPOP_SBC_1 | 75 | 79 | PF00917 | 0.553 |
DOC_CKS1_1 | 448 | 453 | PF01111 | 0.481 |
DOC_CYCLIN_RxL_1 | 276 | 285 | PF00134 | 0.360 |
DOC_MAPK_gen_1 | 14 | 21 | PF00069 | 0.313 |
DOC_MAPK_gen_1 | 280 | 286 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 476 | 486 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 94 | 103 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 338 | 345 | PF00069 | 0.476 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 695 | 699 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 179 | 183 | PF12436 | 0.398 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 652 | 657 | PF00397 | 0.617 |
LIG_14-3-3_CanoR_1 | 14 | 21 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 281 | 287 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 304 | 308 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 642 | 650 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 714 | 722 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 72 | 82 | PF00244 | 0.496 |
LIG_Actin_WH2_2 | 516 | 533 | PF00022 | 0.564 |
LIG_AP2alpha_2 | 86 | 88 | PF02296 | 0.396 |
LIG_BRCT_BRCA1_1 | 214 | 218 | PF00533 | 0.474 |
LIG_Clathr_ClatBox_1 | 18 | 22 | PF01394 | 0.532 |
LIG_Clathr_ClatBox_1 | 315 | 319 | PF01394 | 0.383 |
LIG_deltaCOP1_diTrp_1 | 574 | 582 | PF00928 | 0.526 |
LIG_deltaCOP1_diTrp_1 | 91 | 95 | PF00928 | 0.317 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.490 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.775 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.762 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.522 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.362 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.470 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.402 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.535 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.653 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.607 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.626 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.535 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.492 |
LIG_GBD_Chelix_1 | 152 | 160 | PF00786 | 0.388 |
LIG_Integrin_isoDGR_2 | 412 | 414 | PF01839 | 0.231 |
LIG_LIR_Gen_1 | 441 | 451 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 541 | 552 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 680 | 686 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 91 | 95 | PF02991 | 0.483 |
LIG_NRBOX | 378 | 384 | PF00104 | 0.474 |
LIG_PCNA_yPIPBox_3 | 376 | 386 | PF02747 | 0.456 |
LIG_PCNA_yPIPBox_3 | 393 | 403 | PF02747 | 0.331 |
LIG_PCNA_yPIPBox_3 | 594 | 603 | PF02747 | 0.498 |
LIG_PDZ_Class_1 | 723 | 728 | PF00595 | 0.468 |
LIG_Pex14_2 | 88 | 92 | PF04695 | 0.370 |
LIG_PTB_Apo_2 | 702 | 709 | PF02174 | 0.286 |
LIG_RPA_C_Fungi | 709 | 721 | PF08784 | 0.476 |
LIG_SH2_CRK | 653 | 657 | PF00017 | 0.396 |
LIG_SH2_CRK | 683 | 687 | PF00017 | 0.382 |
LIG_SH2_GRB2like | 591 | 594 | PF00017 | 0.325 |
LIG_SH2_NCK_1 | 584 | 588 | PF00017 | 0.611 |
LIG_SH2_NCK_1 | 653 | 657 | PF00017 | 0.396 |
LIG_SH2_SRC | 265 | 268 | PF00017 | 0.428 |
LIG_SH2_SRC | 584 | 587 | PF00017 | 0.615 |
LIG_SH2_SRC | 666 | 669 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 423 | 427 | PF00017 | 0.270 |
LIG_SH2_STAP1 | 440 | 444 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 544 | 548 | PF00017 | 0.628 |
LIG_SH2_STAT3 | 591 | 594 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 666 | 669 | PF00017 | 0.439 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.500 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.653 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.459 |
LIG_SUMO_SIM_anti_2 | 134 | 140 | PF11976 | 0.265 |
LIG_SUMO_SIM_anti_2 | 16 | 22 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 482 | 487 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 134 | 140 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 16 | 22 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 341 | 347 | PF11976 | 0.396 |
LIG_SUMO_SIM_par_1 | 482 | 487 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 685 | 693 | PF11976 | 0.455 |
LIG_TYR_ITIM | 125 | 130 | PF00017 | 0.356 |
LIG_UBA3_1 | 382 | 386 | PF00899 | 0.360 |
MOD_CDK_SPxxK_3 | 469 | 476 | PF00069 | 0.543 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.354 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.737 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.281 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.712 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.692 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.720 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.266 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.665 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.371 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.708 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.353 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.685 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.231 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.411 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.682 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.728 |
MOD_Cter_Amidation | 328 | 331 | PF01082 | 0.470 |
MOD_Cter_Amidation | 534 | 537 | PF01082 | 0.506 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.443 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.555 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.580 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.373 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.789 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.637 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.561 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.604 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.266 |
MOD_GlcNHglycan | 692 | 695 | PF01048 | 0.459 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.441 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.511 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.785 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.706 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.430 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.704 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.595 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.391 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.505 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.699 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.497 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.719 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.735 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.436 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.414 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.632 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.470 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.302 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.291 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.705 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.542 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.483 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.426 |
MOD_NEK2_2 | 282 | 287 | PF00069 | 0.300 |
MOD_NEK2_2 | 623 | 628 | PF00069 | 0.325 |
MOD_OFUCOSY | 159 | 166 | PF10250 | 0.394 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.281 |
MOD_PIKK_1 | 547 | 553 | PF00454 | 0.480 |
MOD_PK_1 | 200 | 206 | PF00069 | 0.691 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.498 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.588 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.524 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.266 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.511 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.519 |
MOD_PKA_2 | 669 | 675 | PF00069 | 0.622 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.518 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.448 |
MOD_Plk_1 | 670 | 676 | PF00069 | 0.731 |
MOD_Plk_1 | 679 | 685 | PF00069 | 0.564 |
MOD_Plk_2-3 | 134 | 140 | PF00069 | 0.265 |
MOD_Plk_2-3 | 320 | 326 | PF00069 | 0.586 |
MOD_Plk_2-3 | 463 | 469 | PF00069 | 0.519 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.265 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.674 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.571 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.385 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.303 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.294 |
MOD_Plk_4 | 695 | 701 | PF00069 | 0.568 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.418 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.509 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.567 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.679 |
MOD_ProDKin_1 | 652 | 658 | PF00069 | 0.614 |
MOD_SUMO_rev_2 | 180 | 190 | PF00179 | 0.506 |
MOD_SUMO_rev_2 | 487 | 497 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 528 | 538 | PF00179 | 0.559 |
TRG_DiLeu_BaEn_1 | 609 | 614 | PF01217 | 0.300 |
TRG_DiLeu_BaLyEn_6 | 543 | 548 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.642 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.615 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.300 |
TRG_ER_diArg_1 | 478 | 481 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 576 | 579 | PF00400 | 0.671 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 403 | 408 | PF00026 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 546 | 551 | PF00026 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 595 | 599 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA19 | Leptomonas seymouri | 56% | 100% |
A0A0S4KLG2 | Bodo saltans | 35% | 100% |
A0A1X0NSS5 | Trypanosomatidae | 39% | 100% |
A0A3S7WZW4 | Leishmania donovani | 81% | 100% |
A0A422NJ04 | Trypanosoma rangeli | 38% | 100% |
A4I281 | Leishmania infantum | 81% | 100% |
C9ZRR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AYC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q8WR00 | Leishmania major | 79% | 99% |
V5DA92 | Trypanosoma cruzi | 41% | 100% |