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: A4H9K7
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 | 163 | 167 | PF00656 | 0.356 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.311 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 81 | 83 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.297 |
DEG_APCC_DBOX_1 | 244 | 252 | PF00400 | 0.567 |
DOC_CDC14_PxL_1 | 281 | 289 | PF14671 | 0.220 |
DOC_CYCLIN_yCln2_LP_2 | 190 | 196 | PF00134 | 0.343 |
DOC_CYCLIN_yCln2_LP_2 | 347 | 353 | PF00134 | 0.327 |
DOC_CYCLIN_yCln2_LP_2 | 70 | 76 | PF00134 | 0.399 |
DOC_MAPK_gen_1 | 274 | 281 | PF00069 | 0.253 |
DOC_PP1_RVXF_1 | 65 | 72 | PF00149 | 0.321 |
DOC_PP2B_LxvP_1 | 260 | 263 | PF13499 | 0.430 |
DOC_PP2B_LxvP_1 | 51 | 54 | PF13499 | 0.358 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.332 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.328 |
DOC_USP7_UBL2_3 | 389 | 393 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 200 | 208 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 46 | 54 | PF00244 | 0.279 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.234 |
LIG_Clathr_ClatBox_1 | 146 | 150 | PF01394 | 0.392 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.462 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.328 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.603 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.323 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.456 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.303 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.299 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.368 |
LIG_IRF3_LxIS_1 | 73 | 79 | PF10401 | 0.500 |
LIG_LIR_Gen_1 | 211 | 221 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 341 | 351 | PF02991 | 0.177 |
LIG_LIR_Gen_1 | 440 | 448 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 55 | 64 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 391 | 395 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 440 | 444 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.373 |
LIG_NRBOX | 135 | 141 | PF00104 | 0.234 |
LIG_NRBOX | 184 | 190 | PF00104 | 0.327 |
LIG_Pex14_1 | 268 | 272 | PF04695 | 0.283 |
LIG_Pex14_1 | 290 | 294 | PF04695 | 0.292 |
LIG_Pex14_2 | 221 | 225 | PF04695 | 0.467 |
LIG_Pex14_2 | 435 | 439 | PF04695 | 0.308 |
LIG_REV1ctd_RIR_1 | 415 | 421 | PF16727 | 0.450 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.571 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.307 |
LIG_SH2_GRB2like | 214 | 217 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 108 | 112 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 206 | 210 | PF00017 | 0.637 |
LIG_SH2_NCK_1 | 296 | 300 | PF00017 | 0.357 |
LIG_SH2_SRC | 155 | 158 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 11 | 15 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 296 | 300 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.297 |
LIG_SUMO_SIM_anti_2 | 184 | 190 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 192 | 198 | PF11976 | 0.326 |
LIG_SUMO_SIM_anti_2 | 426 | 431 | PF11976 | 0.354 |
LIG_SUMO_SIM_anti_2 | 55 | 61 | PF11976 | 0.167 |
LIG_SUMO_SIM_par_1 | 187 | 192 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 285 | 291 | PF11976 | 0.222 |
LIG_UBA3_1 | 146 | 153 | PF00899 | 0.479 |
LIG_UBA3_1 | 434 | 443 | PF00899 | 0.223 |
MOD_CDK_SPK_2 | 5 | 10 | PF00069 | 0.449 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.329 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.332 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.618 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.318 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.331 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.279 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.575 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.256 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.359 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.578 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.488 |
MOD_GlcNHglycan | 19 | 23 | PF01048 | 0.755 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.295 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.235 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.585 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.642 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.659 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.331 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.335 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.304 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.493 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.528 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.426 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.430 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.265 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.559 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.361 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.279 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.534 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.564 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.327 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.540 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.362 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.362 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.573 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.229 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.478 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.407 |
MOD_PKA_1 | 81 | 87 | PF00069 | 0.558 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.633 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.471 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.558 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.577 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.351 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.351 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.330 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.597 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.289 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.304 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.350 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.292 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.271 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.450 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.235 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.552 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.335 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.328 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.580 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.596 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.635 |
TRG_DiLeu_BaLyEn_6 | 327 | 332 | PF01217 | 0.349 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.291 |
TRG_ER_diArg_1 | 398 | 400 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8S5 | Leptomonas seymouri | 23% | 100% |
A0A0N1IBB8 | Leptomonas seymouri | 60% | 95% |
A0A0N1IHK9 | Leptomonas seymouri | 26% | 100% |
A0A0S4JF45 | Bodo saltans | 38% | 100% |
A0A0S4JH99 | Bodo saltans | 25% | 90% |
A0A0S4JIT1 | Bodo saltans | 23% | 100% |
A0A1X0NN16 | Trypanosomatidae | 23% | 100% |
A0A1X0NQB5 | Trypanosomatidae | 25% | 100% |
A0A1X0P6Z0 | Trypanosomatidae | 45% | 100% |
A0A3Q8IC78 | Leishmania donovani | 26% | 100% |
A0A3Q8IS12 | Leishmania donovani | 24% | 100% |
A0A3R7L1P3 | Trypanosoma rangeli | 25% | 100% |
A0A3S7WUZ5 | Leishmania donovani | 84% | 100% |
A0A422NGL1 | Trypanosoma rangeli | 25% | 100% |
A0A422P0Q3 | Trypanosoma rangeli | 44% | 100% |
A4H690 | Leishmania braziliensis | 26% | 99% |
A4HQI4 | Leishmania braziliensis | 26% | 100% |
A4HUL3 | Leishmania infantum | 26% | 100% |
A4HXX3 | Leishmania infantum | 83% | 100% |
C9ZVP0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZZS9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AHZ3 | Leishmania infantum | 24% | 100% |
E9ANB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9ARN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9AU97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q094 | Leishmania major | 24% | 89% |
Q4QDU2 | Leishmania major | 81% | 98% |
Q4QHB2 | Leishmania major | 25% | 94% |
V5BTU3 | Trypanosoma cruzi | 25% | 100% |
V5DDT9 | Trypanosoma cruzi | 25% | 100% |
V5DN72 | Trypanosoma cruzi | 44% | 100% |