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: E9ANB2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0006862 | nucleotide transport | 6 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0015748 | organophosphate ester transport | 5 | 6 |
GO:0015931 | nucleobase-containing compound transport | 5 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
GO:0055085 | transmembrane transport | 2 | 6 |
GO:0071702 | organic substance transport | 4 | 6 |
GO:0071705 | nitrogen compound transport | 4 | 6 |
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 | 24 | 28 | PF00656 | 0.586 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.295 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.471 |
DEG_APCC_DBOX_1 | 141 | 149 | PF00400 | 0.578 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.677 |
DEG_SCF_FBW7_1 | 333 | 340 | PF00400 | 0.471 |
DOC_CKS1_1 | 334 | 339 | PF01111 | 0.439 |
DOC_CYCLIN_yCln2_LP_2 | 105 | 111 | PF00134 | 0.514 |
DOC_CYCLIN_yCln2_LP_2 | 322 | 328 | PF00134 | 0.305 |
DOC_MAPK_MEF2A_6 | 194 | 202 | PF00069 | 0.428 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.284 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 206 | 213 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 215 | 220 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 229 | 235 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 273 | 280 | PF00244 | 0.462 |
LIG_Actin_WH2_2 | 218 | 234 | PF00022 | 0.527 |
LIG_BRCT_BRCA1_1 | 131 | 135 | PF00533 | 0.467 |
LIG_CtBP_PxDLS_1 | 108 | 112 | PF00389 | 0.471 |
LIG_CtBP_PxDLS_1 | 150 | 154 | PF00389 | 0.356 |
LIG_deltaCOP1_diTrp_1 | 289 | 297 | PF00928 | 0.429 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.510 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.301 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.285 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.439 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.636 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.604 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.723 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.404 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.256 |
LIG_IBAR_NPY_1 | 324 | 326 | PF08397 | 0.439 |
LIG_LIR_Apic_2 | 289 | 295 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 159 | 166 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 378 | 386 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 82 | 91 | PF02991 | 0.517 |
LIG_LIR_LC3C_4 | 240 | 244 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 218 | 222 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.228 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.521 |
LIG_Pex14_1 | 252 | 256 | PF04695 | 0.231 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.343 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.329 |
LIG_SH2_SRC | 15 | 18 | PF00017 | 0.603 |
LIG_SH2_SRC | 264 | 267 | PF00017 | 0.276 |
LIG_SH2_SRC | 379 | 382 | PF00017 | 0.219 |
LIG_SH2_STAP1 | 187 | 191 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.447 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.500 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.777 |
LIG_WRC_WIRS_1 | 259 | 264 | PF05994 | 0.333 |
MOD_CDK_SPxxK_3 | 208 | 215 | PF00069 | 0.387 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.469 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.410 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.312 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.256 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.742 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.728 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.280 |
MOD_GlcNHglycan | 16 | 20 | PF01048 | 0.480 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.566 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.245 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.317 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.568 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.348 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.243 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.722 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.468 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.713 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.604 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.370 |
MOD_N-GLC_2 | 366 | 368 | PF02516 | 0.407 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.539 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.687 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.317 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.302 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.232 |
MOD_NEK2_2 | 230 | 235 | PF00069 | 0.414 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.510 |
MOD_PKA_1 | 115 | 121 | PF00069 | 0.535 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.467 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.338 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.698 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.523 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.403 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.313 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.191 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.341 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.711 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.514 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.506 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.436 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.716 |
TRG_DiLeu_BaEn_4 | 67 | 73 | PF01217 | 0.727 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.228 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 142 | 146 | PF00026 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8S5 | Leptomonas seymouri | 31% | 100% |
A0A0N1IBB8 | Leptomonas seymouri | 23% | 82% |
A0A0N1IHK9 | Leptomonas seymouri | 64% | 100% |
A0A0S4JF45 | Bodo saltans | 29% | 96% |
A0A0S4JH99 | Bodo saltans | 43% | 78% |
A0A0S4JIT1 | Bodo saltans | 30% | 100% |
A0A1X0NN16 | Trypanosomatidae | 31% | 100% |
A0A1X0NQB5 | Trypanosomatidae | 53% | 100% |
A0A1X0P6Z0 | Trypanosomatidae | 26% | 99% |
A0A3Q8IC78 | Leishmania donovani | 94% | 100% |
A0A3Q8IS12 | Leishmania donovani | 30% | 100% |
A0A3R7L1P3 | Trypanosoma rangeli | 28% | 100% |
A0A3S7WUZ5 | Leishmania donovani | 24% | 88% |
A0A422NGL1 | Trypanosoma rangeli | 52% | 100% |
A0A422P0Q3 | Trypanosoma rangeli | 27% | 100% |
A4H690 | Leishmania braziliensis | 79% | 100% |
A4H9K7 | Leishmania braziliensis | 24% | 100% |
A4HQI4 | Leishmania braziliensis | 31% | 100% |
A4HUL3 | Leishmania infantum | 94% | 100% |
A4HXX3 | Leishmania infantum | 24% | 88% |
C9ZVP0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
C9ZZS9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 99% |
E9AHZ3 | Leishmania infantum | 30% | 100% |
E9ARN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AU97 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
Q4Q094 | Leishmania major | 30% | 100% |
Q4QDU2 | Leishmania major | 26% | 100% |
Q4QHB2 | Leishmania major | 88% | 99% |
Q54VX4 | Dictyostelium discoideum | 22% | 100% |
V5BTU3 | Trypanosoma cruzi | 51% | 100% |
V5DDT9 | Trypanosoma cruzi | 29% | 100% |
V5DN72 | Trypanosoma cruzi | 27% | 100% |