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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HHW8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016485 | protein processing | 5 | 1 |
GO:0016539 | intein-mediated protein splicing | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0030908 | protein splicing | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 98 | 102 | PF00656 | 0.558 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.559 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.311 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 326 | 332 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 54 | 58 | PF00082 | 0.586 |
DEG_SCF_FBW7_1 | 198 | 205 | PF00400 | 0.523 |
DEG_SPOP_SBC_1 | 530 | 534 | PF00917 | 0.659 |
DOC_CDC14_PxL_1 | 230 | 238 | PF14671 | 0.544 |
DOC_CKS1_1 | 136 | 141 | PF01111 | 0.630 |
DOC_CKS1_1 | 199 | 204 | PF01111 | 0.532 |
DOC_CKS1_1 | 538 | 543 | PF01111 | 0.405 |
DOC_CYCLIN_RxL_1 | 330 | 341 | PF00134 | 0.547 |
DOC_CYCLIN_RxL_1 | 361 | 372 | PF00134 | 0.397 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.589 |
DOC_MAPK_DCC_7 | 134 | 142 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 247 | 253 | PF00069 | 0.553 |
DOC_MAPK_gen_1 | 266 | 276 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 330 | 340 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 362 | 370 | PF00069 | 0.647 |
DOC_MAPK_gen_1 | 556 | 567 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.392 |
DOC_MAPK_MEF2A_6 | 305 | 312 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 556 | 565 | PF00069 | 0.623 |
DOC_MAPK_RevD_3 | 565 | 580 | PF00069 | 0.524 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.584 |
DOC_PP2B_LxvP_1 | 495 | 498 | PF13499 | 0.515 |
DOC_PP2B_LxvP_1 | 518 | 521 | PF13499 | 0.613 |
DOC_PP4_FxxP_1 | 181 | 184 | PF00568 | 0.395 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.668 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.276 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.442 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.641 |
DOC_USP7_UBL2_3 | 362 | 366 | PF12436 | 0.639 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.316 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.294 |
LIG_14-3-3_CanoR_1 | 213 | 223 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 524 | 530 | PF00244 | 0.631 |
LIG_APCC_ABBA_1 | 419 | 424 | PF00400 | 0.522 |
LIG_BRCT_BRCA1_1 | 164 | 168 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 347 | 351 | PF00533 | 0.476 |
LIG_Clathr_ClatBox_1 | 337 | 341 | PF01394 | 0.456 |
LIG_CSL_BTD_1 | 199 | 202 | PF09270 | 0.416 |
LIG_DLG_GKlike_1 | 95 | 103 | PF00625 | 0.557 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.509 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.463 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.355 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.526 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.351 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.493 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.305 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.423 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.538 |
LIG_HCF-1_HBM_1 | 259 | 262 | PF13415 | 0.409 |
LIG_Integrin_RGD_1 | 580 | 582 | PF01839 | 0.552 |
LIG_LIR_Apic_2 | 16 | 22 | PF02991 | 0.682 |
LIG_LIR_Apic_2 | 217 | 222 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 104 | 113 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 153 | 162 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 403 | 409 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 476 | 485 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 403 | 407 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.428 |
LIG_LYPXL_S_1 | 400 | 404 | PF13949 | 0.481 |
LIG_MYND_1 | 3 | 7 | PF01753 | 0.647 |
LIG_Pex14_1 | 473 | 477 | PF04695 | 0.429 |
LIG_Pex14_2 | 74 | 78 | PF04695 | 0.427 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 219 | 222 | PF00017 | 0.327 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 29 | 33 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 477 | 481 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.475 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.622 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.404 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.695 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.570 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.455 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.532 |
LIG_SUMO_SIM_anti_2 | 566 | 571 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 336 | 341 | PF11976 | 0.535 |
LIG_TRAF2_1 | 504 | 507 | PF00917 | 0.573 |
LIG_TRFH_1 | 453 | 457 | PF08558 | 0.420 |
LIG_WRC_WIRS_1 | 163 | 168 | PF05994 | 0.276 |
LIG_WRC_WIRS_1 | 401 | 406 | PF05994 | 0.582 |
LIG_WW_3 | 8 | 12 | PF00397 | 0.500 |
MOD_CDK_SPK_2 | 537 | 542 | PF00069 | 0.430 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.574 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.446 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.677 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.565 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.647 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.595 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.606 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.442 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.532 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.445 |
MOD_CMANNOS | 285 | 288 | PF00535 | 0.383 |
MOD_Cter_Amidation | 554 | 557 | PF01082 | 0.578 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.588 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.691 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.684 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.510 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.614 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.617 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.516 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.430 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.574 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.636 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.648 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.424 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.289 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.477 |
MOD_N-GLC_2 | 212 | 214 | PF02516 | 0.274 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.437 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.388 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.478 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.361 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.577 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.479 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.618 |
MOD_NEK2_2 | 203 | 208 | PF00069 | 0.560 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.601 |
MOD_PIKK_1 | 436 | 442 | PF00454 | 0.747 |
MOD_PKA_1 | 267 | 273 | PF00069 | 0.547 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.431 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.547 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.666 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.617 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.721 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.602 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.460 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.443 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.511 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.635 |
MOD_Plk_2-3 | 559 | 565 | PF00069 | 0.593 |
MOD_Plk_2-3 | 568 | 574 | PF00069 | 0.483 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.458 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.413 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.442 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.443 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.713 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.551 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.712 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.480 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.517 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.375 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.473 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.610 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.533 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.412 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.310 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.634 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.414 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.299 |
MOD_SUMO_for_1 | 184 | 187 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 126 | 136 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 259 | 269 | PF00179 | 0.431 |
TRG_DiLeu_BaEn_1 | 507 | 512 | PF01217 | 0.385 |
TRG_DiLeu_BaEn_1 | 513 | 518 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_4 | 463 | 469 | PF01217 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 268 | 273 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.392 |
TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 556 | 558 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 577 | 580 | PF00400 | 0.563 |
TRG_NES_CRM1_1 | 509 | 523 | PF08389 | 0.378 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8C2 | Leptomonas seymouri | 66% | 100% |
A0A1X0P2D9 | Trypanosomatidae | 40% | 100% |
A0A3S5IRH4 | Trypanosoma rangeli | 41% | 100% |
A0A3S7X2Z0 | Leishmania donovani | 81% | 100% |
A4I518 | Leishmania infantum | 81% | 100% |
C9ZQH7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9B0E8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q7T5 | Leishmania major | 80% | 100% |
V5BLG2 | Trypanosoma cruzi | 44% | 100% |