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. | yes | yes: 5 |
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4QDJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 10 |
GO:0006720 | isoprenoid metabolic process | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0008299 | isoprenoid biosynthetic process | 4 | 10 |
GO:0008610 | lipid biosynthetic process | 4 | 10 |
GO:0009058 | biosynthetic process | 2 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044249 | cellular biosynthetic process | 3 | 10 |
GO:0044255 | cellular lipid metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901576 | organic substance biosynthetic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004659 | prenyltransferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016765 | transferase activity, transferring alkyl or aryl (other than methyl) groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 14 | 18 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 285 | 289 | PF00656 | 0.469 |
CLV_C14_Caspase3-7 | 488 | 492 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 570 | 574 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 579 | 583 | PF00656 | 0.410 |
CLV_C14_Caspase3-7 | 647 | 651 | PF00656 | 0.377 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 676 | 678 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 739 | 741 | PF00675 | 0.444 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.377 |
CLV_PCSK_PC1ET2_1 | 137 | 139 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.456 |
DEG_APCC_DBOX_1 | 668 | 676 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 706 | 714 | PF00400 | 0.569 |
DOC_MAPK_gen_1 | 111 | 118 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 445 | 455 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 496 | 504 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 535 | 544 | PF00069 | 0.402 |
DOC_MAPK_HePTP_8 | 108 | 120 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 111 | 120 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 616 | 625 | PF00069 | 0.518 |
DOC_MAPK_NFAT4_5 | 616 | 624 | PF00069 | 0.518 |
DOC_MAPK_RevD_3 | 726 | 741 | PF00069 | 0.433 |
DOC_PP4_FxxP_1 | 520 | 523 | PF00568 | 0.462 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.424 |
DOC_USP7_MATH_2 | 532 | 538 | PF00917 | 0.518 |
LIG_14-3-3_CanoR_1 | 166 | 171 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 319 | 327 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 382 | 391 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 445 | 451 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 669 | 673 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 731 | 737 | PF00244 | 0.539 |
LIG_Actin_WH2_2 | 109 | 127 | PF00022 | 0.518 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.717 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 574 | 578 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 699 | 703 | PF00533 | 0.490 |
LIG_deltaCOP1_diTrp_1 | 3 | 9 | PF00928 | 0.701 |
LIG_eIF4E_1 | 559 | 565 | PF01652 | 0.477 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.405 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.487 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.609 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.517 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.496 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.581 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.436 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.353 |
LIG_FHA_2 | 574 | 580 | PF00498 | 0.518 |
LIG_LIR_Apic_2 | 562 | 566 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 19 | 27 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 214 | 222 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 250 | 261 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 304 | 312 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 575 | 584 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 671 | 679 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 712 | 721 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 732 | 738 | PF02991 | 0.209 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 29 | 35 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 449 | 453 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 575 | 581 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 671 | 676 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 712 | 717 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 722 | 728 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 732 | 736 | PF02991 | 0.209 |
LIG_NBox_RRM_1 | 617 | 627 | PF00076 | 0.455 |
LIG_NRBOX | 119 | 125 | PF00104 | 0.518 |
LIG_Pex14_1 | 5 | 9 | PF04695 | 0.634 |
LIG_Pex14_2 | 51 | 55 | PF04695 | 0.379 |
LIG_REV1ctd_RIR_1 | 369 | 379 | PF16727 | 0.474 |
LIG_REV1ctd_RIR_1 | 53 | 61 | PF16727 | 0.434 |
LIG_SH2_GRB2like | 34 | 37 | PF00017 | 0.377 |
LIG_SH2_PTP2 | 216 | 219 | PF00017 | 0.456 |
LIG_SH2_PTP2 | 472 | 475 | PF00017 | 0.402 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.518 |
LIG_SH2_SRC | 394 | 397 | PF00017 | 0.526 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 71 | 75 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.193 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 519 | 522 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.402 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.449 |
LIG_SUMO_SIM_anti_2 | 117 | 122 | PF11976 | 0.456 |
LIG_SUMO_SIM_anti_2 | 452 | 457 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 452 | 457 | PF11976 | 0.391 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.565 |
LIG_TYR_ITSM | 212 | 219 | PF00017 | 0.462 |
LIG_UBA3_1 | 120 | 126 | PF00899 | 0.477 |
LIG_UBA3_1 | 78 | 85 | PF00899 | 0.518 |
LIG_WRC_WIRS_1 | 308 | 313 | PF05994 | 0.402 |
LIG_WRC_WIRS_1 | 52 | 57 | PF05994 | 0.434 |
LIG_WRC_WIRS_1 | 730 | 735 | PF05994 | 0.418 |
LIG_WW_3 | 9 | 13 | PF00397 | 0.659 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.423 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.376 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.518 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.382 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.586 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.477 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.582 |
MOD_Cter_Amidation | 109 | 112 | PF01082 | 0.481 |
MOD_GlcNHglycan | 162 | 166 | PF01048 | 0.455 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.610 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.516 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.518 |
MOD_GlcNHglycan | 356 | 360 | PF01048 | 0.498 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.487 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.432 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.475 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.374 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.456 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.452 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.421 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.386 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.374 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.518 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.497 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.472 |
MOD_N-GLC_1 | 382 | 387 | PF02516 | 0.553 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.291 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.518 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.444 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.518 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.397 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.471 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.487 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.391 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.483 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.410 |
MOD_NEK2_2 | 37 | 42 | PF00069 | 0.456 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.477 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.518 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.477 |
MOD_PKA_1 | 166 | 172 | PF00069 | 0.466 |
MOD_PKA_1 | 677 | 683 | PF00069 | 0.476 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.661 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.503 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.512 |
MOD_PKA_2 | 668 | 674 | PF00069 | 0.470 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.466 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.435 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.484 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.518 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.398 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.394 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.518 |
MOD_Plk_1 | 721 | 727 | PF00069 | 0.508 |
MOD_Plk_2-3 | 573 | 579 | PF00069 | 0.518 |
MOD_Plk_2-3 | 93 | 99 | PF00069 | 0.518 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.424 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.381 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.370 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.477 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.437 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.377 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.362 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.365 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.377 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.518 |
MOD_Plk_4 | 605 | 611 | PF00069 | 0.456 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.526 |
MOD_Plk_4 | 732 | 738 | PF00069 | 0.498 |
MOD_SUMO_for_1 | 222 | 225 | PF00179 | 0.518 |
MOD_SUMO_for_1 | 41 | 44 | PF00179 | 0.518 |
MOD_SUMO_for_1 | 641 | 644 | PF00179 | 0.456 |
MOD_SUMO_rev_2 | 242 | 250 | PF00179 | 0.691 |
MOD_SUMO_rev_2 | 644 | 654 | PF00179 | 0.400 |
TRG_DiLeu_BaEn_4 | 400 | 406 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 131 | 136 | PF01217 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 716 | 721 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 470 | 472 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 707 | 710 | PF00400 | 0.536 |
TRG_ER_FFAT_2 | 19 | 29 | PF00635 | 0.415 |
TRG_NES_CRM1_1 | 477 | 488 | PF08389 | 0.377 |
TRG_NES_CRM1_1 | 685 | 697 | PF08389 | 0.476 |
TRG_NLS_MonoExtN_4 | 134 | 141 | PF00514 | 0.291 |
TRG_Pf-PMV_PEXEL_1 | 280 | 284 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 440 | 444 | PF00026 | 0.359 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IRK5 | Bodo saltans | 48% | 94% |
A0A1X0P7U9 | Trypanosomatidae | 50% | 100% |
A0A3S7WV99 | Leishmania donovani | 94% | 100% |
A0A422ND06 | Trypanosoma rangeli | 51% | 99% |
A4H9X9 | Leishmania braziliensis | 80% | 100% |
A4HY44 | Leishmania infantum | 94% | 100% |
E9ARX3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5C1S4 | Trypanosoma cruzi | 43% | 99% |