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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9AI92
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 5 |
GO:0022857 | transmembrane transporter activity | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.756 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.690 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.617 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.569 |
DEG_SPOP_SBC_1 | 332 | 336 | PF00917 | 0.430 |
DOC_MAPK_gen_1 | 168 | 175 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 233 | 241 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 236 | 243 | PF00069 | 0.546 |
DOC_PP2B_LxvP_1 | 258 | 261 | PF13499 | 0.444 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.391 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 140 | 144 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 146 | 156 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 441 | 447 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 456 | 460 | PF00244 | 0.619 |
LIG_APCC_ABBA_1 | 435 | 440 | PF00400 | 0.645 |
LIG_APCC_ABBAyCdc20_2 | 456 | 462 | PF00400 | 0.641 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.630 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.665 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.725 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.757 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.742 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.619 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.662 |
LIG_LIR_Apic_2 | 232 | 238 | PF02991 | 0.598 |
LIG_LIR_Apic_2 | 295 | 301 | PF02991 | 0.670 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.646 |
LIG_LIR_Gen_1 | 171 | 179 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 188 | 197 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 155 | 159 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 171 | 175 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 188 | 192 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 272 | 276 | PF02991 | 0.375 |
LIG_NRP_CendR_1 | 503 | 505 | PF00754 | 0.586 |
LIG_Pex14_2 | 273 | 277 | PF04695 | 0.411 |
LIG_SH2_CRK | 235 | 239 | PF00017 | 0.524 |
LIG_SH2_SRC | 223 | 226 | PF00017 | 0.244 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.815 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.411 |
LIG_SH3_1 | 68 | 74 | PF00018 | 0.654 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.769 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.604 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.633 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.722 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.757 |
LIG_SUMO_SIM_par_1 | 317 | 322 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 340 | 346 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 72 | 81 | PF11976 | 0.655 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.662 |
LIG_TRAF2_1 | 431 | 434 | PF00917 | 0.712 |
LIG_UBA3_1 | 253 | 259 | PF00899 | 0.411 |
LIG_WRC_WIRS_1 | 153 | 158 | PF05994 | 0.622 |
LIG_WRC_WIRS_1 | 186 | 191 | PF05994 | 0.244 |
LIG_WRC_WIRS_1 | 270 | 275 | PF05994 | 0.411 |
MOD_CDC14_SPxK_1 | 104 | 107 | PF00782 | 0.644 |
MOD_CDK_SPxK_1 | 101 | 107 | PF00069 | 0.648 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.381 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.350 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.411 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.688 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.639 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.627 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.831 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.712 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.602 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.783 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.561 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.274 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.361 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.634 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.566 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.538 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.545 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.468 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.443 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.532 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.518 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.786 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.482 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.775 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.631 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.692 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.747 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.465 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.627 |
MOD_N-GLC_2 | 314 | 316 | PF02516 | 0.411 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.349 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.389 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.411 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.400 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.522 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.656 |
MOD_NEK2_2 | 353 | 358 | PF00069 | 0.244 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.674 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.667 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.624 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.676 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.584 |
MOD_PKA_1 | 441 | 447 | PF00069 | 0.810 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.704 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.682 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.653 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.666 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.760 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.810 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.658 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.578 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.682 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.436 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.411 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.410 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.362 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.377 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.362 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.388 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.761 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.648 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.427 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.633 |
MOD_SUMO_rev_2 | 422 | 431 | PF00179 | 0.636 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.595 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 502 | 505 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.664 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I416 | Leptomonas seymouri | 52% | 71% |
A0A3Q8IBI9 | Leishmania donovani | 69% | 69% |
A4HYN7 | Leishmania infantum | 69% | 69% |
E9AUH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 70% |
Q4QD06 | Leishmania major | 70% | 100% |