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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4QCJ4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.542 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.307 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.611 |
DEG_APCC_DBOX_1 | 389 | 397 | PF00400 | 0.565 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.630 |
DOC_CYCLIN_RxL_1 | 374 | 385 | PF00134 | 0.407 |
DOC_CYCLIN_yCln2_LP_2 | 267 | 273 | PF00134 | 0.446 |
DOC_MAPK_DCC_7 | 221 | 229 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 141 | 147 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 221 | 229 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 245 | 253 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 304 | 312 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 376 | 383 | PF00069 | 0.436 |
DOC_MAPK_gen_1 | 522 | 531 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 179 | 186 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 222 | 231 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 246 | 255 | PF00069 | 0.376 |
DOC_MAPK_MEF2A_6 | 376 | 383 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 525 | 533 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 70 | 77 | PF00069 | 0.338 |
DOC_MAPK_NFAT4_5 | 376 | 384 | PF00069 | 0.441 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.431 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.741 |
LIG_14-3-3_CanoR_1 | 376 | 380 | PF00244 | 0.460 |
LIG_BIR_III_2 | 249 | 253 | PF00653 | 0.426 |
LIG_BRCT_BRCA1_1 | 421 | 425 | PF00533 | 0.458 |
LIG_Clathr_ClatBox_1 | 407 | 411 | PF01394 | 0.455 |
LIG_CtBP_PxDLS_1 | 217 | 223 | PF00389 | 0.417 |
LIG_deltaCOP1_diTrp_1 | 266 | 271 | PF00928 | 0.554 |
LIG_deltaCOP1_diTrp_1 | 482 | 488 | PF00928 | 0.496 |
LIG_EVH1_1 | 431 | 435 | PF00568 | 0.611 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.571 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.401 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.459 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.510 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.573 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.677 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.444 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.521 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.471 |
LIG_GBD_Chelix_1 | 379 | 387 | PF00786 | 0.447 |
LIG_GBD_Chelix_1 | 400 | 408 | PF00786 | 0.374 |
LIG_LIR_Apic_2 | 363 | 369 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 483 | 494 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.430 |
LIG_LYPXL_SIV_4 | 338 | 346 | PF13949 | 0.383 |
LIG_NRBOX | 382 | 388 | PF00104 | 0.406 |
LIG_NRBOX | 399 | 405 | PF00104 | 0.283 |
LIG_NRBOX | 73 | 79 | PF00104 | 0.444 |
LIG_PCNA_yPIPBox_3 | 389 | 399 | PF02747 | 0.459 |
LIG_RPA_C_Fungi | 372 | 384 | PF08784 | 0.332 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.445 |
LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.520 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.445 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.457 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.475 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.394 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.667 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.629 |
LIG_SUMO_SIM_anti_2 | 394 | 400 | PF11976 | 0.384 |
LIG_SUMO_SIM_anti_2 | 405 | 412 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 69 | 76 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 182 | 187 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 227 | 235 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 405 | 412 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 73 | 79 | PF11976 | 0.408 |
LIG_TRAF2_1 | 480 | 483 | PF00917 | 0.349 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.324 |
LIG_TYR_ITIM | 81 | 86 | PF00017 | 0.323 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.390 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.538 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.447 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.492 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.469 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.429 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.430 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.529 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.661 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.574 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.606 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.461 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.573 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.560 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.551 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.518 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.383 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.701 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.612 |
MOD_N-GLC_2 | 309 | 311 | PF02516 | 0.284 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.510 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.383 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.479 |
MOD_NEK2_2 | 216 | 221 | PF00069 | 0.491 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.469 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.469 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.471 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.576 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.500 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.414 |
MOD_Plk_1 | 482 | 488 | PF00069 | 0.534 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.520 |
MOD_Plk_2-3 | 515 | 521 | PF00069 | 0.445 |
MOD_Plk_2-3 | 88 | 94 | PF00069 | 0.473 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.457 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.511 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.516 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.414 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.462 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.561 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.614 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.741 |
MOD_SUMO_for_1 | 92 | 95 | PF00179 | 0.428 |
TRG_DiLeu_BaEn_1 | 394 | 399 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 163 | 168 | PF01217 | 0.476 |
TRG_DiLeu_BaLyEn_6 | 329 | 334 | PF01217 | 0.399 |
TRG_DiLeu_BaLyEn_6 | 366 | 371 | PF01217 | 0.345 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 220 | 223 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.462 |
TRG_NES_CRM1_1 | 397 | 411 | PF08389 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I200 | Leptomonas seymouri | 44% | 90% |
A0A0S4IXJ4 | Bodo saltans | 25% | 100% |
A0A3R7KNI1 | Trypanosoma rangeli | 31% | 89% |
A0A3S5H793 | Leishmania donovani | 94% | 100% |
A4HBM0 | Leishmania braziliensis | 78% | 100% |
A4HZA8 | Leishmania infantum | 94% | 100% |
E9AUY8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5DGY6 | Trypanosoma cruzi | 30% | 100% |