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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4HLJ2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.547 |
CLV_PCSK_KEX2_1 | 165 | 167 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 165 | 167 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.662 |
DEG_APCC_DBOX_1 | 240 | 248 | PF00400 | 0.463 |
DEG_APCC_DBOX_1 | 418 | 426 | PF00400 | 0.452 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.421 |
DOC_ANK_TNKS_1 | 268 | 275 | PF00023 | 0.526 |
DOC_CKS1_1 | 345 | 350 | PF01111 | 0.660 |
DOC_CYCLIN_RxL_1 | 292 | 301 | PF00134 | 0.442 |
DOC_MAPK_gen_1 | 180 | 188 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 419 | 427 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 180 | 188 | PF00069 | 0.550 |
DOC_MAPK_MEF2A_6 | 419 | 427 | PF00069 | 0.564 |
DOC_PP2B_LxvP_1 | 446 | 449 | PF13499 | 0.615 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.553 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.626 |
DOC_USP7_UBL2_3 | 125 | 129 | PF12436 | 0.355 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 109 | 117 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 280 | 287 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 395 | 401 | PF00244 | 0.601 |
LIG_BRCT_BRCA1_1 | 360 | 364 | PF00533 | 0.663 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.477 |
LIG_Clathr_ClatBox_1 | 275 | 279 | PF01394 | 0.592 |
LIG_deltaCOP1_diTrp_1 | 4 | 12 | PF00928 | 0.587 |
LIG_deltaCOP1_diTrp_1 | 424 | 433 | PF00928 | 0.580 |
LIG_eIF4E_1 | 270 | 276 | PF01652 | 0.525 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.507 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.741 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.570 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.659 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.553 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.527 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.637 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.642 |
LIG_GBD_Chelix_1 | 203 | 211 | PF00786 | 0.321 |
LIG_LIR_Apic_2 | 267 | 273 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 11 | 15 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 122 | 126 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.559 |
LIG_PCNA_yPIPBox_3 | 137 | 151 | PF02747 | 0.400 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.711 |
LIG_RPA_C_Fungi | 191 | 203 | PF08784 | 0.405 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.476 |
LIG_SH2_CRK | 270 | 274 | PF00017 | 0.523 |
LIG_SH2_CRK | 382 | 386 | PF00017 | 0.537 |
LIG_SH2_NCK_1 | 123 | 127 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 266 | 270 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 398 | 402 | PF00017 | 0.564 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.568 |
LIG_SH3_1 | 259 | 265 | PF00018 | 0.532 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.568 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.611 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.614 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.603 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.465 |
LIG_TRAF2_1 | 24 | 27 | PF00917 | 0.471 |
LIG_TRAF2_2 | 24 | 29 | PF00917 | 0.471 |
LIG_TYR_ITIM | 96 | 101 | PF00017 | 0.321 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.554 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.436 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.541 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.605 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.573 |
MOD_CMANNOS | 314 | 317 | PF00535 | 0.567 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.582 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.575 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.512 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.512 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.582 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.441 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.551 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.643 |
MOD_N-GLC_1 | 58 | 63 | PF02516 | 0.534 |
MOD_N-GLC_2 | 80 | 82 | PF02516 | 0.416 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.401 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.547 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.530 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.631 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.573 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.381 |
MOD_NEK2_2 | 293 | 298 | PF00069 | 0.433 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.375 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.559 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.444 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.582 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.591 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.557 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.648 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.576 |
MOD_Plk_2-3 | 25 | 31 | PF00069 | 0.564 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.604 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.520 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.441 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.529 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.657 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.566 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.520 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.623 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.524 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.605 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.667 |
MOD_SUMO_rev_2 | 39 | 47 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_2 | 428 | 434 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 346 | 351 | PF01217 | 0.630 |
TRG_DiLeu_BaLyEn_6 | 64 | 69 | PF01217 | 0.593 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.380 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 420 | 424 | PF00026 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 66 | 70 | PF00026 | 0.721 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGZ4 | Leptomonas seymouri | 58% | 70% |
A0A3Q8ID98 | Leishmania donovani | 30% | 72% |
A0A3Q8IM92 | Leishmania donovani | 79% | 67% |
A4H7X2 | Leishmania braziliensis | 31% | 100% |
A4HLI8 | Leishmania braziliensis | 90% | 100% |
A4HLJ0 | Leishmania braziliensis | 92% | 100% |
A4HW99 | Leishmania infantum | 30% | 72% |
A4I8Z8 | Leishmania infantum | 79% | 67% |
E9APZ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 72% |
E9B3W7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 67% |
Q4Q457 | Leishmania major | 79% | 100% |
Q4QFI2 | Leishmania major | 30% | 100% |