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:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 33 |
GO:0110165 | cellular anatomical entity | 1 | 33 |
Related structures:
AlphaFold database: Q4QDU2
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:0035352 | NAD transmembrane transport | 4 | 2 |
GO:0043132 | NAD transport | 7 | 2 |
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:1901679 | nucleotide transmembrane transport | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 2 |
GO:0015215 | nucleotide transmembrane transporter activity | 4 | 2 |
GO:0015605 | organophosphate ester transmembrane transporter activity | 3 | 2 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:0051724 | NAD transmembrane transporter activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.361 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.320 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.304 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.299 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.580 |
DOC_CYCLIN_yCln2_LP_2 | 188 | 194 | PF00134 | 0.361 |
DOC_CYCLIN_yCln2_LP_2 | 337 | 343 | PF00134 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 68 | 74 | PF00134 | 0.411 |
DOC_MAPK_gen_1 | 272 | 279 | PF00069 | 0.270 |
DOC_PP1_RVXF_1 | 239 | 245 | PF00149 | 0.580 |
DOC_PP2B_LxvP_1 | 258 | 261 | PF13499 | 0.444 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.361 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.353 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.590 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 198 | 206 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 378 | 383 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 44 | 52 | PF00244 | 0.283 |
LIG_Actin_WH2_2 | 147 | 162 | PF00022 | 0.419 |
LIG_BRCT_BRCA1_1 | 141 | 145 | PF00533 | 0.256 |
LIG_BRCT_BRCA1_1 | 384 | 388 | PF00533 | 0.543 |
LIG_Clathr_ClatBox_1 | 144 | 148 | PF01394 | 0.411 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.353 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.446 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.325 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.583 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.381 |
LIG_IRF3_LxIS_1 | 71 | 77 | PF10401 | 0.509 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 43 | 52 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 430 | 438 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 53 | 62 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 218 | 222 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 421 | 427 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.385 |
LIG_NRBOX | 133 | 139 | PF00104 | 0.256 |
LIG_NRBOX | 182 | 188 | PF00104 | 0.351 |
LIG_PALB2_WD40_1 | 50 | 58 | PF16756 | 0.317 |
LIG_Pex14_1 | 266 | 270 | PF04695 | 0.299 |
LIG_Pex14_1 | 288 | 292 | PF04695 | 0.293 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.471 |
LIG_Pex14_2 | 425 | 429 | PF04695 | 0.333 |
LIG_REV1ctd_RIR_1 | 405 | 413 | PF16727 | 0.468 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.513 |
LIG_SH2_CRK | 212 | 216 | PF00017 | 0.578 |
LIG_SH2_CRK | 250 | 254 | PF00017 | 0.332 |
LIG_SH2_NCK_1 | 204 | 208 | PF00017 | 0.631 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.405 |
LIG_SH2_SRC | 153 | 156 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.300 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.432 |
LIG_SUMO_SIM_anti_2 | 182 | 188 | PF11976 | 0.372 |
LIG_SUMO_SIM_anti_2 | 190 | 196 | PF11976 | 0.344 |
LIG_SUMO_SIM_anti_2 | 416 | 421 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 185 | 190 | PF11976 | 0.341 |
LIG_TRAF2_2 | 9 | 14 | PF00917 | 0.369 |
LIG_UBA3_1 | 144 | 151 | PF00899 | 0.487 |
LIG_WW_1 | 9 | 12 | PF00397 | 0.370 |
MOD_CDK_SPxxK_3 | 371 | 378 | PF00069 | 0.406 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.346 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.618 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.304 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.395 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.573 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.355 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.505 |
MOD_GlcNHglycan | 20 | 24 | PF01048 | 0.743 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.344 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.667 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.255 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.665 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.351 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.329 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.277 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.488 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.539 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.553 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.443 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.288 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.571 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.498 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.368 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.293 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.567 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.351 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.548 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.385 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.384 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.579 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.498 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.494 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.245 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.486 |
MOD_PKA_1 | 378 | 384 | PF00069 | 0.406 |
MOD_PKA_1 | 79 | 85 | PF00069 | 0.561 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.561 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.375 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.406 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.375 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.355 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.601 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.317 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.295 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.556 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.252 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.559 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.360 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.359 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.473 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.592 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.586 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.632 |
MOD_SUMO_rev_2 | 300 | 305 | PF00179 | 0.330 |
TRG_DiLeu_BaLyEn_6 | 317 | 322 | PF01217 | 0.411 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.316 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8S5 | Leptomonas seymouri | 24% | 100% |
A0A0N1IBB8 | Leptomonas seymouri | 58% | 93% |
A0A0N1IHK9 | Leptomonas seymouri | 26% | 100% |
A0A0S4JF45 | Bodo saltans | 37% | 100% |
A0A0S4JH99 | Bodo saltans | 27% | 88% |
A0A0S4JIT1 | Bodo saltans | 26% | 100% |
A0A1X0NN16 | Trypanosomatidae | 24% | 100% |
A0A1X0NQB5 | Trypanosomatidae | 26% | 100% |
A0A1X0P6Z0 | Trypanosomatidae | 44% | 100% |
A0A3Q8IC78 | Leishmania donovani | 27% | 100% |
A0A3Q8IS12 | Leishmania donovani | 26% | 100% |
A0A3R7L1P3 | Trypanosoma rangeli | 24% | 100% |
A0A3S7WUZ5 | Leishmania donovani | 94% | 100% |
A0A422NGL1 | Trypanosoma rangeli | 25% | 100% |
A0A422P0Q3 | Trypanosoma rangeli | 45% | 100% |
A4H690 | Leishmania braziliensis | 27% | 100% |
A4H9K7 | Leishmania braziliensis | 81% | 98% |
A4HQI4 | Leishmania braziliensis | 27% | 100% |
A4HUL3 | Leishmania infantum | 26% | 100% |
A4HXX3 | Leishmania infantum | 94% | 100% |
C9ZVP0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
C9ZZS9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AHZ3 | Leishmania infantum | 26% | 100% |
E9ANB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ARN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AU97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q094 | Leishmania major | 26% | 92% |
Q4QHB2 | Leishmania major | 27% | 100% |
V5BTU3 | Trypanosoma cruzi | 26% | 100% |
V5DDT9 | Trypanosoma cruzi | 24% | 100% |
V5DN72 | Trypanosoma cruzi | 46% | 100% |