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 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HV38
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.435 |
DOC_CYCLIN_RxL_1 | 127 | 136 | PF00134 | 0.392 |
DOC_MAPK_gen_1 | 287 | 295 | PF00069 | 0.576 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.477 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.563 |
DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.413 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.422 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 111 | 116 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 127 | 133 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 227 | 236 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 385 | 395 | PF00244 | 0.567 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.656 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.335 |
LIG_Clathr_ClatBox_1 | 334 | 338 | PF01394 | 0.362 |
LIG_eIF4E_1 | 330 | 336 | PF01652 | 0.298 |
LIG_eIF4E_1 | 401 | 407 | PF01652 | 0.471 |
LIG_eIF4E_1 | 62 | 68 | PF01652 | 0.312 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.483 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.635 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.290 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.628 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.269 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.555 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.513 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.485 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.536 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.150 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.459 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.582 |
LIG_LIR_Gen_1 | 408 | 414 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.372 |
LIG_LYPXL_SIV_4 | 256 | 264 | PF13949 | 0.266 |
LIG_MLH1_MIPbox_1 | 113 | 117 | PF16413 | 0.335 |
LIG_NRBOX | 190 | 196 | PF00104 | 0.224 |
LIG_PTB_Apo_2 | 120 | 127 | PF02174 | 0.275 |
LIG_RPA_C_Fungi | 194 | 206 | PF08784 | 0.504 |
LIG_SH2_CRK | 226 | 230 | PF00017 | 0.393 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.431 |
LIG_SH2_CRK | 395 | 399 | PF00017 | 0.368 |
LIG_SH2_PTP2 | 401 | 404 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 211 | 215 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.459 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.400 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.378 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.453 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.385 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.480 |
LIG_SUMO_SIM_anti_2 | 300 | 307 | PF11976 | 0.337 |
LIG_SUMO_SIM_anti_2 | 333 | 338 | PF11976 | 0.359 |
LIG_SUMO_SIM_anti_2 | 428 | 436 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 102 | 107 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 198 | 204 | PF11976 | 0.622 |
LIG_SUMO_SIM_par_1 | 33 | 39 | PF11976 | 0.266 |
LIG_SUMO_SIM_par_1 | 333 | 338 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 428 | 436 | PF11976 | 0.377 |
LIG_TRAF2_1 | 351 | 354 | PF00917 | 0.488 |
LIG_TYR_ITIM | 224 | 229 | PF00017 | 0.224 |
LIG_TYR_ITIM | 399 | 404 | PF00017 | 0.326 |
LIG_UBA3_1 | 369 | 378 | PF00899 | 0.383 |
LIG_WRC_WIRS_1 | 437 | 442 | PF05994 | 0.665 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.249 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.521 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.357 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.343 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.465 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.496 |
MOD_GlcNHglycan | 146 | 150 | PF01048 | 0.530 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.331 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.420 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.532 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.410 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.525 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.368 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.454 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.420 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.411 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.550 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.552 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.316 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.337 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.288 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.335 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.418 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.248 |
MOD_N-GLC_1 | 417 | 422 | PF02516 | 0.249 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.413 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.344 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.240 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.306 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.426 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.494 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.293 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.344 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.478 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.366 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.367 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.322 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.372 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.281 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.438 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.485 |
MOD_PK_1 | 4 | 10 | PF00069 | 0.679 |
MOD_PK_1 | 400 | 406 | PF00069 | 0.489 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.313 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.364 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.431 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.267 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.306 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.453 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.368 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.351 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.269 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.194 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.426 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.463 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.692 |
MOD_SUMO_rev_2 | 298 | 304 | PF00179 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 21 | 26 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.372 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.422 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBZ5 | Leptomonas seymouri | 51% | 100% |
A0A1X0NUV1 | Trypanosomatidae | 25% | 95% |
A0A3Q8I960 | Leishmania donovani | 99% | 100% |
A0A3R7NA95 | Trypanosoma rangeli | 24% | 100% |
A4H6Q3 | Leishmania braziliensis | 72% | 100% |
D0A7B3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 96% |
E9ANR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QGV0 | Leishmania major | 90% | 100% |
V5C1D7 | Trypanosoma cruzi | 25% | 95% |