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 | yes | yes: 6, no: 3 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A0A3Q8ICS7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.487 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.563 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.517 |
DEG_APCC_DBOX_1 | 136 | 144 | PF00400 | 0.544 |
DEG_APCC_DBOX_1 | 284 | 292 | PF00400 | 0.492 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.518 |
DOC_CKS1_1 | 256 | 261 | PF01111 | 0.605 |
DOC_CKS1_1 | 58 | 63 | PF01111 | 0.539 |
DOC_MAPK_HePTP_8 | 8 | 20 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 11 | 20 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 233 | 242 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 73 | 82 | PF00069 | 0.392 |
DOC_MAPK_RevD_3 | 77 | 93 | PF00069 | 0.442 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.446 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.443 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.540 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.540 |
LIG_14-3-3_CanoR_1 | 119 | 123 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 137 | 141 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 223 | 230 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 279 | 288 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 385 | 389 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 55 | 59 | PF00244 | 0.548 |
LIG_Actin_WH2_2 | 136 | 153 | PF00022 | 0.449 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.349 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.471 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.530 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.390 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.558 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.463 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.540 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.586 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.560 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 254 | 259 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.466 |
LIG_LIR_LC3C_4 | 236 | 240 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.564 |
LIG_NRP_CendR_1 | 449 | 450 | PF00754 | 0.498 |
LIG_Pex14_2 | 342 | 346 | PF04695 | 0.577 |
LIG_PTAP_UEV_1 | 354 | 359 | PF05743 | 0.483 |
LIG_PTB_Apo_2 | 177 | 184 | PF02174 | 0.668 |
LIG_PTB_Phospho_1 | 177 | 183 | PF10480 | 0.476 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.523 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.417 |
LIG_SH2_CRK | 369 | 373 | PF00017 | 0.570 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 443 | 447 | PF00017 | 0.499 |
LIG_SH2_STAT3 | 295 | 298 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.573 |
LIG_SH3_2 | 355 | 360 | PF14604 | 0.482 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.504 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.580 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.495 |
LIG_SUMO_SIM_anti_2 | 236 | 242 | PF11976 | 0.455 |
LIG_SUMO_SIM_anti_2 | 318 | 324 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 238 | 244 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 78 | 84 | PF11976 | 0.446 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.481 |
LIG_TYR_ITSM | 159 | 166 | PF00017 | 0.495 |
MOD_CDK_SPK_2 | 255 | 260 | PF00069 | 0.558 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.639 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.489 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.660 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.623 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.604 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.514 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.406 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.628 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.491 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.582 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.503 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.533 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.503 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.672 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.652 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.548 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.523 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.573 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.681 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.541 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.551 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.471 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.399 |
MOD_N-GLC_1 | 179 | 184 | PF02516 | 0.671 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.687 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.507 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.423 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.663 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.603 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.655 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.635 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.592 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.634 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.406 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.594 |
MOD_NEK2_2 | 280 | 285 | PF00069 | 0.558 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.524 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.497 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.583 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.693 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.555 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.392 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.673 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.512 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.522 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.667 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.609 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.560 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.556 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.636 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.550 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.542 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.495 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.470 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4P2 | Leptomonas seymouri | 37% | 97% |
A0A1X0NSG2 | Trypanosomatidae | 21% | 100% |
A0A3R7NPG1 | Trypanosoma rangeli | 24% | 100% |
A4HEQ1 | Leishmania braziliensis | 72% | 100% |
A4I1Y1 | Leishmania infantum | 100% | 100% |
C9ZS38 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AY27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q9E6 | Leishmania major | 90% | 100% |