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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9ATP1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 137 | 141 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.546 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.450 |
DEG_APCC_DBOX_1 | 93 | 101 | PF00400 | 0.546 |
DEG_MDM2_SWIB_1 | 308 | 315 | PF02201 | 0.368 |
DOC_ANK_TNKS_1 | 135 | 142 | PF00023 | 0.432 |
DOC_MAPK_gen_1 | 122 | 131 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 91 | 100 | PF00069 | 0.542 |
DOC_PP1_RVXF_1 | 61 | 67 | PF00149 | 0.524 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.745 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.684 |
LIG_14-3-3_CanoR_1 | 34 | 42 | PF00244 | 0.579 |
LIG_Actin_WH2_1 | 122 | 138 | PF00022 | 0.423 |
LIG_Actin_WH2_2 | 123 | 138 | PF00022 | 0.472 |
LIG_Actin_WH2_2 | 211 | 228 | PF00022 | 0.366 |
LIG_APCC_ABBA_1 | 123 | 128 | PF00400 | 0.383 |
LIG_APCC_ABBA_1 | 266 | 271 | PF00400 | 0.397 |
LIG_APCC_ABBAyCdc20_2 | 122 | 128 | PF00400 | 0.363 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.590 |
LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.443 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.474 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.562 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.373 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.492 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.612 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.458 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.558 |
LIG_GBD_Chelix_1 | 296 | 304 | PF00786 | 0.469 |
LIG_LIR_Gen_1 | 106 | 117 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 164 | 173 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 271 | 278 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 282 | 292 | PF02991 | 0.427 |
LIG_LIR_LC3C_4 | 127 | 131 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 271 | 275 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 282 | 287 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 306 | 311 | PF02991 | 0.404 |
LIG_PDZ_Class_2 | 319 | 324 | PF00595 | 0.432 |
LIG_Pex14_2 | 308 | 312 | PF04695 | 0.366 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.529 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.535 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.548 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.454 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.451 |
LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.465 |
LIG_TYR_ITSM | 280 | 287 | PF00017 | 0.461 |
LIG_WRC_WIRS_1 | 8 | 13 | PF05994 | 0.438 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.418 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.478 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.468 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.628 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.517 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.537 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.632 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.412 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.736 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.506 |
MOD_Cter_Amidation | 45 | 48 | PF01082 | 0.483 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.458 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.697 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.531 |
MOD_GlcNHglycan | 178 | 182 | PF01048 | 0.535 |
MOD_GlcNHglycan | 194 | 198 | PF01048 | 0.327 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.567 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.370 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.681 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.445 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.622 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.377 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.617 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.690 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.458 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.549 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.686 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.639 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.572 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.567 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.417 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.259 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.271 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.545 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.469 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.348 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.464 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.356 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.397 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.686 |
MOD_SUMO_rev_2 | 145 | 151 | PF00179 | 0.483 |
TRG_DiLeu_BaEn_1 | 60 | 65 | PF01217 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 209 | 214 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 99 | 104 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.542 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 212 | 217 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7P6 | Leptomonas seymouri | 35% | 100% |
A0A3S7XBN8 | Leishmania donovani | 83% | 100% |
A4HPX5 | Leishmania braziliensis | 60% | 100% |
A4IDN6 | Leishmania infantum | 83% | 100% |
Q4Q0V7 | Leishmania major | 81% | 100% |