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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4H6Q3
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.308 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.377 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.487 |
DOC_CYCLIN_RxL_1 | 127 | 136 | PF00134 | 0.480 |
DOC_CYCLIN_RxL_1 | 190 | 200 | PF00134 | 0.464 |
DOC_PP1_RVXF_1 | 128 | 134 | PF00149 | 0.324 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.588 |
DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.447 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.443 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 111 | 116 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 206 | 214 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 385 | 392 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 400 | 405 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 413 | 421 | PF00244 | 0.474 |
LIG_BIR_III_4 | 354 | 358 | PF00653 | 0.486 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.421 |
LIG_Clathr_ClatBox_1 | 334 | 338 | PF01394 | 0.480 |
LIG_eIF4E_1 | 401 | 407 | PF01652 | 0.531 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.632 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.330 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.680 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.586 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.639 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.521 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.575 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.335 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.464 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.593 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.298 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.461 |
LIG_LIR_Gen_1 | 223 | 234 | PF02991 | 0.570 |
LIG_LIR_Gen_1 | 408 | 414 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 408 | 412 | PF02991 | 0.524 |
LIG_MLH1_MIPbox_1 | 113 | 117 | PF16413 | 0.421 |
LIG_Pex14_2 | 117 | 121 | PF04695 | 0.333 |
LIG_PTB_Apo_2 | 120 | 127 | PF02174 | 0.313 |
LIG_RPA_C_Fungi | 194 | 206 | PF08784 | 0.623 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 421 | 425 | PF00017 | 0.424 |
LIG_SH2_PTP2 | 401 | 404 | PF00017 | 0.484 |
LIG_SH2_PTP2 | 409 | 412 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.461 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.455 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.473 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.427 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.527 |
LIG_SUMO_SIM_anti_2 | 22 | 28 | PF11976 | 0.354 |
LIG_SUMO_SIM_anti_2 | 300 | 307 | PF11976 | 0.441 |
LIG_SUMO_SIM_anti_2 | 333 | 338 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 100 | 107 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 198 | 204 | PF11976 | 0.615 |
LIG_SUMO_SIM_par_1 | 333 | 338 | PF11976 | 0.446 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.546 |
LIG_TYR_ITIM | 399 | 404 | PF00017 | 0.412 |
LIG_WRC_WIRS_1 | 437 | 442 | PF05994 | 0.683 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.406 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.650 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.612 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.412 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.434 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.374 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.458 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.598 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.400 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.541 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.421 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.548 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.585 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.474 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.387 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.480 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.274 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.291 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.335 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.333 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.546 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.399 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.347 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.534 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.345 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.351 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.413 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.413 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.363 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.411 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.150 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.534 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.540 |
MOD_PK_1 | 400 | 406 | PF00069 | 0.506 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.515 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.227 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.487 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.281 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.465 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.403 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.395 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.382 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.311 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.225 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.429 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.480 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.456 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.372 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.633 |
TRG_DiLeu_BaEn_3 | 300 | 306 | PF01217 | 0.208 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.280 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBZ5 | Leptomonas seymouri | 52% | 100% |
A0A1X0NUV1 | Trypanosomatidae | 25% | 95% |
A0A3Q8I960 | Leishmania donovani | 72% | 100% |
A0A3R7NA95 | Trypanosoma rangeli | 24% | 100% |
A4HV38 | Leishmania infantum | 72% | 100% |
D0A7B3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 96% |
E9ANR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4QGV0 | Leishmania major | 74% | 100% |
V5C1D7 | Trypanosoma cruzi | 24% | 95% |