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: 32 |
NetGPI | no | yes: 0, no: 32 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 33 |
GO:0110165 | cellular anatomical entity | 1 | 33 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HXX3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0006862 | nucleotide transport | 6 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0015748 | organophosphate ester transport | 5 | 7 |
GO:0015931 | nucleobase-containing compound transport | 5 | 7 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
GO:0055085 | transmembrane transport | 2 | 7 |
GO:0071702 | organic substance transport | 4 | 7 |
GO:0071705 | nitrogen compound transport | 4 | 7 |
GO:0035352 | NAD transmembrane transport | 4 | 1 |
GO:0043132 | NAD transport | 7 | 1 |
GO:1901679 | nucleotide transmembrane transport | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0015215 | nucleotide transmembrane transporter activity | 4 | 1 |
GO:0015605 | organophosphate ester transmembrane transporter activity | 3 | 1 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
GO:0051724 | NAD transmembrane transporter activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.342 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.300 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.285 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.282 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.562 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.485 |
DEG_SPOP_SBC_1 | 3 | 7 | PF00917 | 0.334 |
DOC_CYCLIN_yCln2_LP_2 | 188 | 194 | PF00134 | 0.335 |
DOC_CYCLIN_yCln2_LP_2 | 337 | 343 | PF00134 | 0.327 |
DOC_CYCLIN_yCln2_LP_2 | 69 | 75 | PF00134 | 0.388 |
DOC_MAPK_gen_1 | 272 | 279 | PF00069 | 0.248 |
DOC_PP2B_LxvP_1 | 258 | 261 | PF13499 | 0.430 |
DOC_PP2B_LxvP_1 | 50 | 53 | PF13499 | 0.348 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.328 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.617 |
LIG_14-3-3_CanoR_1 | 198 | 206 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 378 | 383 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 45 | 53 | PF00244 | 0.272 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.234 |
LIG_BRCT_BRCA1_1 | 384 | 388 | PF00533 | 0.530 |
LIG_Clathr_ClatBox_1 | 145 | 149 | PF01394 | 0.390 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.328 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.430 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.299 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.387 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.365 |
LIG_IRF3_LxIS_1 | 72 | 78 | PF10401 | 0.491 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 430 | 438 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 54 | 63 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 218 | 222 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 54 | 59 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 67 | 73 | PF02991 | 0.373 |
LIG_NRBOX | 134 | 140 | PF00104 | 0.234 |
LIG_NRBOX | 182 | 188 | PF00104 | 0.327 |
LIG_PALB2_WD40_1 | 51 | 59 | PF16756 | 0.301 |
LIG_Pex14_1 | 266 | 270 | PF04695 | 0.284 |
LIG_Pex14_1 | 288 | 292 | PF04695 | 0.282 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.459 |
LIG_Pex14_2 | 425 | 429 | PF04695 | 0.308 |
LIG_REV1ctd_RIR_1 | 405 | 413 | PF16727 | 0.450 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.496 |
LIG_SH2_CRK | 212 | 216 | PF00017 | 0.564 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.307 |
LIG_SH2_GRB2like | 212 | 215 | PF00017 | 0.578 |
LIG_SH2_NCK_1 | 204 | 208 | PF00017 | 0.633 |
LIG_SH2_NCK_1 | 212 | 216 | PF00017 | 0.446 |
LIG_SH2_SRC | 10 | 13 | PF00017 | 0.380 |
LIG_SH2_SRC | 154 | 157 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.278 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.422 |
LIG_SUMO_SIM_anti_2 | 182 | 188 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 190 | 196 | PF11976 | 0.317 |
LIG_SUMO_SIM_anti_2 | 416 | 421 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 185 | 190 | PF11976 | 0.316 |
LIG_UBA3_1 | 145 | 152 | PF00899 | 0.476 |
MOD_CDC14_SPxK_1 | 159 | 162 | PF00782 | 0.291 |
MOD_CDK_SPK_2 | 156 | 161 | PF00069 | 0.274 |
MOD_CDK_SPK_2 | 4 | 9 | PF00069 | 0.405 |
MOD_CDK_SPxK_1 | 156 | 162 | PF00069 | 0.273 |
MOD_CDK_SPxxK_3 | 371 | 378 | PF00069 | 0.394 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.326 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.612 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.279 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.377 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.567 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.516 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.342 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.486 |
MOD_GlcNHglycan | 18 | 22 | PF01048 | 0.726 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.615 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.329 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.295 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.235 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.648 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.335 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.304 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.459 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.523 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.532 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.404 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.416 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.265 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.565 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.524 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.356 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.279 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.548 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.327 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.534 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.458 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.362 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.356 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.566 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.477 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.229 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.468 |
MOD_PKA_1 | 378 | 384 | PF00069 | 0.413 |
MOD_PKA_1 | 80 | 86 | PF00069 | 0.542 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.613 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.542 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.351 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.394 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.351 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.330 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.292 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.271 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.546 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.235 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.542 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.354 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.335 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.340 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.590 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.554 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.620 |
MOD_SUMO_rev_2 | 300 | 305 | PF00179 | 0.316 |
TRG_DiLeu_BaLyEn_6 | 317 | 322 | PF01217 | 0.402 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.291 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 79 | 82 | PF00400 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8S5 | Leptomonas seymouri | 25% | 100% |
A0A0N1IBB8 | Leptomonas seymouri | 59% | 93% |
A0A0N1IHK9 | Leptomonas seymouri | 26% | 100% |
A0A0S4JF45 | Bodo saltans | 37% | 100% |
A0A0S4JH99 | Bodo saltans | 26% | 88% |
A0A0S4JIT1 | Bodo saltans | 24% | 100% |
A0A1X0NN16 | Trypanosomatidae | 23% | 100% |
A0A1X0NQB5 | Trypanosomatidae | 26% | 100% |
A0A1X0P6Z0 | Trypanosomatidae | 45% | 100% |
A0A3Q8IC78 | Leishmania donovani | 26% | 100% |
A0A3Q8IS12 | Leishmania donovani | 26% | 100% |
A0A3R7L1P3 | Trypanosoma rangeli | 24% | 100% |
A0A3S7WUZ5 | Leishmania donovani | 100% | 100% |
A0A422NGL1 | Trypanosoma rangeli | 25% | 100% |
A0A422P0Q3 | Trypanosoma rangeli | 46% | 100% |
A4H690 | Leishmania braziliensis | 26% | 100% |
A4H9K7 | Leishmania braziliensis | 83% | 100% |
A4HQI4 | Leishmania braziliensis | 26% | 88% |
A4HUL3 | Leishmania infantum | 24% | 98% |
C9ZVP0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZZS9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AHZ3 | Leishmania infantum | 26% | 100% |
E9ANB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 97% |
E9ARN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AU97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 92% |
Q4Q094 | Leishmania major | 26% | 92% |
Q4QDU2 | Leishmania major | 94% | 100% |
Q4QHB2 | Leishmania major | 26% | 97% |
V5BTU3 | Trypanosoma cruzi | 26% | 100% |
V5DDT9 | Trypanosoma cruzi | 24% | 100% |
V5DN72 | Trypanosoma cruzi | 45% | 100% |