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 |
Related structures:
AlphaFold database: Q4QIQ2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.564 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.380 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.437 |
CLV_PCSK_PC7_1 | 477 | 483 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.656 |
CLV_Separin_Metazoa | 360 | 364 | PF03568 | 0.665 |
DEG_Kelch_Keap1_1 | 205 | 210 | PF01344 | 0.547 |
DOC_MAPK_FxFP_2 | 238 | 241 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 155 | 161 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 424 | 434 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 155 | 163 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 252 | 260 | PF00069 | 0.534 |
DOC_PP1_RVXF_1 | 111 | 118 | PF00149 | 0.558 |
DOC_PP4_FxxP_1 | 238 | 241 | PF00568 | 0.510 |
DOC_SPAK_OSR1_1 | 341 | 345 | PF12202 | 0.419 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.615 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 156 | 162 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 191 | 199 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 411 | 419 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 44 | 54 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 72 | 80 | PF00244 | 0.647 |
LIG_APCC_ABBA_1 | 432 | 437 | PF00400 | 0.331 |
LIG_BIR_III_2 | 135 | 139 | PF00653 | 0.483 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.648 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.331 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.517 |
LIG_Clathr_ClatBox_1 | 399 | 403 | PF01394 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 35 | 43 | PF00928 | 0.603 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.666 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.570 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.344 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.511 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.495 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.659 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.449 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.443 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.475 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.376 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.533 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.615 |
LIG_HCF-1_HBM_1 | 405 | 408 | PF13415 | 0.411 |
LIG_Integrin_isoDGR_2 | 350 | 352 | PF01839 | 0.540 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 380 | 389 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 167 | 171 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 316 | 320 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 380 | 384 | PF02991 | 0.302 |
LIG_PCNA_yPIPBox_3 | 191 | 202 | PF02747 | 0.476 |
LIG_PCNA_yPIPBox_3 | 44 | 58 | PF02747 | 0.588 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.553 |
LIG_SH2_GRB2like | 317 | 320 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.321 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.476 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.579 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.428 |
LIG_TRAF2_1 | 353 | 356 | PF00917 | 0.612 |
LIG_WRC_WIRS_1 | 146 | 151 | PF05994 | 0.458 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.647 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.596 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.433 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.273 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.511 |
MOD_Cter_Amidation | 153 | 156 | PF01082 | 0.468 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.539 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.703 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.595 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.431 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.600 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.393 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.602 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.584 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.411 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.448 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.566 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.457 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.411 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.650 |
MOD_N-GLC_1 | 492 | 497 | PF02516 | 0.506 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.484 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.497 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.528 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.597 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.531 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.393 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.677 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.477 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.611 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.560 |
MOD_PK_1 | 93 | 99 | PF00069 | 0.549 |
MOD_PKA_1 | 155 | 161 | PF00069 | 0.470 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.489 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.560 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.470 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.579 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.454 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.477 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.539 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.409 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.393 |
MOD_Plk_1 | 492 | 498 | PF00069 | 0.482 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.568 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.537 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.436 |
MOD_SUMO_for_1 | 491 | 494 | PF00179 | 0.579 |
MOD_SUMO_rev_2 | 147 | 157 | PF00179 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.281 |
TRG_ER_diArg_1 | 475 | 477 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 479 | 482 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 504 | 507 | PF00400 | 0.551 |
TRG_NES_CRM1_1 | 364 | 377 | PF08389 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 113 | 118 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 261 | 266 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 363 | 367 | PF00026 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 398 | 403 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.366 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9I2 | Leptomonas seymouri | 72% | 99% |
A0A0S4ILP7 | Bodo saltans | 40% | 100% |
A0A1X0NPY0 | Trypanosomatidae | 49% | 100% |
A0A3R7KA86 | Trypanosoma rangeli | 51% | 100% |
A0A3S7WPU9 | Leishmania donovani | 98% | 100% |
A4H4Y7 | Leishmania braziliensis | 85% | 100% |
C9ZUR3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AG73 | Leishmania infantum | 98% | 100% |
E9AL52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5D8S1 | Trypanosoma cruzi | 49% | 100% |