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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: E9B3F0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0008643 | carbohydrate transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.305 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.241 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.318 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.298 |
DEG_APCC_DBOX_1 | 300 | 308 | PF00400 | 0.439 |
DEG_APCC_DBOX_1 | 65 | 73 | PF00400 | 0.498 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.429 |
DOC_CYCLIN_RxL_1 | 188 | 199 | PF00134 | 0.481 |
DOC_CYCLIN_RxL_1 | 23 | 34 | PF00134 | 0.239 |
DOC_CYCLIN_yCln2_LP_2 | 334 | 340 | PF00134 | 0.192 |
DOC_MAPK_DCC_7 | 26 | 35 | PF00069 | 0.239 |
DOC_MAPK_FxFP_2 | 259 | 262 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 65 | 71 | PF00069 | 0.493 |
DOC_MAPK_HePTP_8 | 351 | 363 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 297 | 306 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 354 | 363 | PF00069 | 0.366 |
DOC_MAPK_RevD_3 | 422 | 437 | PF00069 | 0.238 |
DOC_PP2B_LxvP_1 | 111 | 114 | PF13499 | 0.353 |
DOC_PP2B_LxvP_1 | 334 | 337 | PF13499 | 0.192 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.324 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.253 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.434 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 301 | 305 | PF00244 | 0.498 |
LIG_Actin_WH2_2 | 180 | 198 | PF00022 | 0.423 |
LIG_APCC_ABBA_1 | 59 | 64 | PF00400 | 0.482 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.216 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.498 |
LIG_eIF4E_1 | 319 | 325 | PF01652 | 0.353 |
LIG_eIF4E_1 | 81 | 87 | PF01652 | 0.303 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.512 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.415 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.393 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.321 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.347 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.281 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.348 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.480 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.498 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.498 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.263 |
LIG_GBD_Chelix_1 | 174 | 182 | PF00786 | 0.281 |
LIG_GBD_Chelix_1 | 416 | 424 | PF00786 | 0.249 |
LIG_IRF3_LxIS_1 | 389 | 396 | PF10401 | 0.303 |
LIG_LIR_Apic_2 | 45 | 50 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 236 | 245 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 303 | 314 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 345 | 356 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 375 | 385 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 407 | 417 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 82 | 90 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 236 | 240 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 303 | 308 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 375 | 380 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.298 |
LIG_MLH1_MIPbox_1 | 103 | 107 | PF16413 | 0.216 |
LIG_MLH1_MIPbox_1 | 302 | 306 | PF16413 | 0.498 |
LIG_NRBOX | 161 | 167 | PF00104 | 0.249 |
LIG_Pex14_1 | 315 | 319 | PF04695 | 0.303 |
LIG_Pex14_2 | 261 | 265 | PF04695 | 0.284 |
LIG_PTB_Apo_2 | 260 | 267 | PF02174 | 0.361 |
LIG_PTB_Phospho_1 | 260 | 266 | PF10480 | 0.349 |
LIG_SH2_PTP2 | 112 | 115 | PF00017 | 0.353 |
LIG_SH2_PTP2 | 341 | 344 | PF00017 | 0.298 |
LIG_SH2_SRC | 254 | 257 | PF00017 | 0.326 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.298 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.345 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.337 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.342 |
LIG_SUMO_SIM_anti_2 | 3 | 10 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 160 | 167 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 231 | 236 | PF11976 | 0.183 |
LIG_SUMO_SIM_par_1 | 3 | 10 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 414 | 419 | PF11976 | 0.358 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.498 |
LIG_TRAF2_1 | 292 | 295 | PF00917 | 0.498 |
LIG_TRFH_1 | 84 | 88 | PF08558 | 0.303 |
LIG_UBA3_1 | 394 | 400 | PF00899 | 0.249 |
LIG_WRC_WIRS_1 | 234 | 239 | PF05994 | 0.183 |
LIG_WRC_WIRS_1 | 344 | 349 | PF05994 | 0.270 |
MOD_CDK_SPK_2 | 186 | 191 | PF00069 | 0.434 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.353 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.357 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.399 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.331 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.352 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.366 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.353 |
MOD_CMANNOS | 213 | 216 | PF00535 | 0.333 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.353 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.221 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.422 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.490 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.183 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.310 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.366 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.366 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.548 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.358 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.406 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.379 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.414 |
MOD_N-GLC_2 | 269 | 271 | PF02516 | 0.353 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.332 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.362 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.584 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.400 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.365 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.224 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.298 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.426 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.391 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.414 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.365 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.341 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.360 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.330 |
MOD_NEK2_2 | 164 | 169 | PF00069 | 0.432 |
MOD_NEK2_2 | 343 | 348 | PF00069 | 0.336 |
MOD_NEK2_2 | 79 | 84 | PF00069 | 0.211 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.353 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.443 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.270 |
MOD_PIKK_1 | 407 | 413 | PF00454 | 0.281 |
MOD_PKA_1 | 290 | 296 | PF00069 | 0.249 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.324 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.252 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.601 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.400 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.311 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.569 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.443 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.319 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.294 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.303 |
MOD_Plk_2-3 | 373 | 379 | PF00069 | 0.311 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.398 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.353 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.352 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.396 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.364 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.373 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.346 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.304 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.353 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.355 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.353 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.384 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.306 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.303 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.361 |
TRG_NES_CRM1_1 | 49 | 64 | PF08389 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 222 | 227 | PF00026 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 26 | 31 | PF00026 | 0.270 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYC7 | Leptomonas seymouri | 24% | 83% |
A0A0N1I3H1 | Leptomonas seymouri | 65% | 67% |
A0A3Q8IF44 | Leishmania donovani | 25% | 84% |
A0A3Q8ILR5 | Leishmania donovani | 88% | 97% |
A4HIW8 | Leishmania braziliensis | 25% | 100% |
A4HL09 | Leishmania braziliensis | 79% | 100% |
A4I8J0 | Leishmania infantum | 88% | 97% |
E9AHK6 | Leishmania infantum | 25% | 84% |
E9B1F2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
F4KIL8 | Arabidopsis thaliana | 22% | 93% |
Q4Q4Q0 | Leishmania major | 87% | 100% |
Q4Q6R0 | Leishmania major | 26% | 100% |
Q55721 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 24% | 93% |
Q5FV41 | Arabidopsis thaliana | 22% | 92% |
Q9SKZ5 | Arabidopsis thaliana | 23% | 82% |
Q9SQN2 | Arabidopsis thaliana | 22% | 92% |