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: E9ARN7
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 | 295 | 299 | PF00656 | 0.365 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.322 |
CLV_PCSK_KEX2_1 | 390 | 392 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 83 | 85 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.302 |
DEG_APCC_DBOX_1 | 246 | 254 | PF00400 | 0.581 |
DEG_SCF_FBW7_1 | 1 | 7 | PF00400 | 0.363 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.364 |
DOC_CYCLIN_yCln2_LP_2 | 192 | 198 | PF00134 | 0.362 |
DOC_CYCLIN_yCln2_LP_2 | 341 | 347 | PF00134 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 72 | 78 | PF00134 | 0.414 |
DOC_MAPK_gen_1 | 276 | 283 | PF00069 | 0.266 |
DOC_PP2B_LxvP_1 | 262 | 265 | PF13499 | 0.444 |
DOC_PP2B_LxvP_1 | 53 | 56 | PF13499 | 0.360 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.353 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.590 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.605 |
LIG_14-3-3_CanoR_1 | 202 | 210 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 382 | 387 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 48 | 56 | PF00244 | 0.328 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.256 |
LIG_Clathr_ClatBox_1 | 148 | 152 | PF01394 | 0.412 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.353 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.458 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.324 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.397 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.376 |
LIG_IRF3_LxIS_1 | 75 | 81 | PF10401 | 0.511 |
LIG_LIR_Gen_1 | 213 | 223 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 335 | 345 | PF02991 | 0.185 |
LIG_LIR_Gen_1 | 431 | 439 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 47 | 56 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 222 | 226 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 431 | 435 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.403 |
LIG_NRBOX | 137 | 143 | PF00104 | 0.256 |
LIG_NRBOX | 186 | 192 | PF00104 | 0.351 |
LIG_PALB2_WD40_1 | 54 | 62 | PF16756 | 0.317 |
LIG_Pex14_1 | 270 | 274 | PF04695 | 0.298 |
LIG_Pex14_1 | 292 | 296 | PF04695 | 0.300 |
LIG_Pex14_2 | 223 | 227 | PF04695 | 0.472 |
LIG_Pex14_2 | 426 | 430 | PF04695 | 0.333 |
LIG_REV1ctd_RIR_1 | 406 | 414 | PF16727 | 0.468 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.500 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.563 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.332 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.631 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.413 |
LIG_SH2_SRC | 157 | 160 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.296 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.430 |
LIG_SUMO_SIM_anti_2 | 186 | 192 | PF11976 | 0.372 |
LIG_SUMO_SIM_anti_2 | 194 | 200 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 417 | 422 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 189 | 194 | PF11976 | 0.341 |
LIG_UBA3_1 | 148 | 155 | PF00899 | 0.457 |
LIG_WRPW_2 | 386 | 389 | PF00400 | 0.356 |
MOD_CDC14_SPxK_1 | 236 | 239 | PF00782 | 0.489 |
MOD_CDK_SPK_2 | 159 | 164 | PF00069 | 0.289 |
MOD_CDK_SPK_2 | 375 | 380 | PF00069 | 0.356 |
MOD_CDK_SPK_2 | 7 | 12 | PF00069 | 0.468 |
MOD_CDK_SPxK_1 | 233 | 239 | PF00069 | 0.480 |
MOD_CDK_SPxxK_3 | 375 | 382 | PF00069 | 0.406 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.346 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.618 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.381 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.326 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.573 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.387 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.561 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.352 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.503 |
MOD_GlcNHglycan | 21 | 25 | PF01048 | 0.751 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.348 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.320 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.255 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.664 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.358 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.499 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.329 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.494 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.539 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.552 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.423 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.537 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.287 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.440 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.571 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.288 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.363 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.562 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.351 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.550 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.375 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.383 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.579 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.494 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.245 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.488 |
MOD_PKA_1 | 382 | 388 | PF00069 | 0.406 |
MOD_PKA_1 | 83 | 89 | PF00069 | 0.564 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.627 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.564 |
MOD_PKB_1 | 380 | 388 | PF00069 | 0.519 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.375 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.406 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.375 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.355 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.624 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.318 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.294 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.247 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.563 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.381 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.360 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.574 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.350 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.592 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.595 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.608 |
MOD_SUMO_rev_2 | 304 | 309 | PF00179 | 0.343 |
TRG_DiLeu_BaLyEn_6 | 321 | 326 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.316 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 389 | 391 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8S5 | Leptomonas seymouri | 25% | 100% |
A0A0N1IBB8 | Leptomonas seymouri | 59% | 93% |
A0A0N1IHK9 | Leptomonas seymouri | 27% | 100% |
A0A0S4JF45 | Bodo saltans | 37% | 100% |
A0A0S4JH99 | Bodo saltans | 27% | 88% |
A0A0S4JIT1 | Bodo saltans | 23% | 100% |
A0A1X0NN16 | Trypanosomatidae | 23% | 100% |
A0A1X0NQB5 | Trypanosomatidae | 26% | 100% |
A0A1X0P6Z0 | Trypanosomatidae | 46% | 100% |
A0A3Q8IC78 | Leishmania donovani | 26% | 100% |
A0A3Q8IS12 | Leishmania donovani | 27% | 100% |
A0A3R7L1P3 | Trypanosoma rangeli | 24% | 100% |
A0A3S7WUZ5 | Leishmania donovani | 93% | 100% |
A0A422NGL1 | Trypanosoma rangeli | 26% | 100% |
A0A422P0Q3 | Trypanosoma rangeli | 44% | 100% |
A4H690 | Leishmania braziliensis | 27% | 100% |
A4H9K7 | Leishmania braziliensis | 83% | 100% |
A4HQI4 | Leishmania braziliensis | 26% | 89% |
A4HUL3 | Leishmania infantum | 26% | 100% |
A4HXX3 | Leishmania infantum | 93% | 100% |
C9ZVP0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZZS9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AHZ3 | Leishmania infantum | 27% | 100% |
E9ANB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AU97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q094 | Leishmania major | 26% | 93% |
Q4QDU2 | Leishmania major | 89% | 99% |
Q4QHB2 | Leishmania major | 26% | 97% |
V5BTU3 | Trypanosoma cruzi | 26% | 100% |
V5DDT9 | Trypanosoma cruzi | 24% | 100% |
V5DN72 | Trypanosoma cruzi | 46% | 100% |