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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ARM4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 375 | 379 | PF00656 | 0.609 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.674 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 421 | 423 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 491 | 497 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.428 |
DEG_APCC_DBOX_1 | 485 | 493 | PF00400 | 0.473 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.520 |
DEG_SPOP_SBC_1 | 412 | 416 | PF00917 | 0.607 |
DOC_ANK_TNKS_1 | 494 | 501 | PF00023 | 0.516 |
DOC_CYCLIN_RxL_1 | 105 | 118 | PF00134 | 0.592 |
DOC_MAPK_gen_1 | 105 | 114 | PF00069 | 0.639 |
DOC_MAPK_gen_1 | 486 | 494 | PF00069 | 0.476 |
DOC_MAPK_HePTP_8 | 7 | 19 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 10 | 19 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 149 | 156 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 246 | 253 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 30 | 37 | PF00069 | 0.327 |
DOC_MAPK_MEF2A_6 | 343 | 352 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 354 | 361 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 57 | 66 | PF00069 | 0.498 |
DOC_MAPK_NFAT4_5 | 246 | 254 | PF00069 | 0.288 |
DOC_MAPK_RevD_3 | 492 | 508 | PF00069 | 0.374 |
DOC_PP4_FxxP_1 | 253 | 256 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 516 | 519 | PF00568 | 0.386 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.657 |
DOC_USP7_UBL2_3 | 428 | 432 | PF12436 | 0.652 |
DOC_USP7_UBL2_3 | 503 | 507 | PF12436 | 0.492 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.702 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 188 | 195 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 207 | 212 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 272 | 281 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 400 | 409 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 427 | 436 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 91 | 95 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 69 | 87 | PF00022 | 0.434 |
LIG_BIR_III_4 | 169 | 173 | PF00653 | 0.463 |
LIG_BRCT_BRCA1_1 | 78 | 82 | PF00533 | 0.352 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.502 |
LIG_CtBP_PxDLS_1 | 4 | 8 | PF00389 | 0.451 |
LIG_EH1_1 | 459 | 467 | PF00400 | 0.474 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.462 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.396 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.446 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.452 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.317 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.507 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.328 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.347 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.484 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.623 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.420 |
LIG_LIR_Apic_2 | 513 | 519 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 123 | 133 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.374 |
LIG_MYND_3 | 498 | 502 | PF01753 | 0.510 |
LIG_NRBOX | 488 | 494 | PF00104 | 0.522 |
LIG_PDZ_Class_1 | 520 | 525 | PF00595 | 0.426 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.508 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 166 | 170 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 512 | 516 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.329 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.582 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.426 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.582 |
LIG_SUMO_SIM_anti_2 | 347 | 353 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 455 | 461 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 518 | 523 | PF11976 | 0.370 |
LIG_TYR_ITIM | 20 | 25 | PF00017 | 0.510 |
MOD_CDK_SPK_2 | 100 | 105 | PF00069 | 0.589 |
MOD_CDK_SPK_2 | 52 | 57 | PF00069 | 0.634 |
MOD_CDK_SPxK_1 | 201 | 207 | PF00069 | 0.686 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.759 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.554 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.578 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.632 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.693 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.680 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.449 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.772 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.690 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.521 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.657 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.503 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.477 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.639 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.561 |
MOD_Cter_Amidation | 425 | 428 | PF01082 | 0.573 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.467 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.663 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.681 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.683 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.676 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.665 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.583 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.389 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.676 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.598 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.495 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.478 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.563 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.754 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.485 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.622 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.318 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.759 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.502 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.477 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.590 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.544 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.699 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.677 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.405 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.502 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.692 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.800 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.374 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.381 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.645 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.508 |
MOD_PKA_1 | 393 | 399 | PF00069 | 0.700 |
MOD_PKA_1 | 427 | 433 | PF00069 | 0.616 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.673 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.444 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.378 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.747 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.716 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.514 |
MOD_PKB_1 | 108 | 116 | PF00069 | 0.675 |
MOD_PKB_1 | 425 | 433 | PF00069 | 0.568 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.319 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.528 |
MOD_Plk_2-3 | 320 | 326 | PF00069 | 0.610 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.539 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.511 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.385 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.508 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.644 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.346 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.707 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.645 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.699 |
MOD_SUMO_rev_2 | 363 | 371 | PF00179 | 0.470 |
TRG_DiLeu_BaEn_4 | 303 | 309 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 488 | 493 | PF01217 | 0.521 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.367 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 206 | 209 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 110 | 115 | PF00026 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 232 | 236 | PF00026 | 0.314 |
TRG_PTS1 | 522 | 525 | PF00515 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMJ2 | Leptomonas seymouri | 53% | 90% |
A0A1X0P774 | Trypanosomatidae | 31% | 100% |
A0A3Q8IB16 | Leishmania donovani | 88% | 98% |
A4H9J5 | Leishmania braziliensis | 72% | 100% |
A4HXW1 | Leishmania infantum | 89% | 98% |
C9ZZU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4QDV5 | Leishmania major | 88% | 100% |