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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9APX8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.685 |
CLV_MEL_PAP_1 | 254 | 260 | PF00089 | 0.441 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.531 |
DEG_COP1_1 | 285 | 294 | PF00400 | 0.610 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.556 |
DOC_CKS1_1 | 327 | 332 | PF01111 | 0.541 |
DOC_MAPK_gen_1 | 123 | 132 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 298 | 306 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 72 | 81 | PF00069 | 0.434 |
DOC_MAPK_HePTP_8 | 204 | 216 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 207 | 216 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 298 | 306 | PF00069 | 0.402 |
DOC_PP1_MyPhoNE_1 | 298 | 305 | PF00149 | 0.461 |
DOC_PP1_RVXF_1 | 9 | 16 | PF00149 | 0.586 |
DOC_PP2B_LxvP_1 | 243 | 246 | PF13499 | 0.465 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.495 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 107 | 117 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 174 | 178 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 197 | 204 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 280 | 287 | PF00244 | 0.686 |
LIG_BRCT_BRCA1_1 | 156 | 160 | PF00533 | 0.597 |
LIG_CaM_IQ_9 | 248 | 264 | PF13499 | 0.428 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.491 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.394 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.594 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.679 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.554 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.529 |
LIG_PTAP_UEV_1 | 165 | 170 | PF05743 | 0.531 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.484 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.473 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.536 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.689 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.684 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.567 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.565 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.481 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.519 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.457 |
MOD_CDK_SPxxK_3 | 326 | 333 | PF00069 | 0.463 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.610 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.634 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.600 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.635 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.514 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.689 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.468 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.601 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.629 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.639 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.708 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.416 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.486 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.645 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.515 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.606 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.463 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.567 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.653 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.595 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.510 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.438 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.631 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.545 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.657 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.601 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.693 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.576 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.587 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.637 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.521 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.714 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.542 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.431 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.627 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.710 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.377 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.584 |
MOD_PK_1 | 307 | 313 | PF00069 | 0.438 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.603 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.519 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.614 |
MOD_PKB_1 | 107 | 115 | PF00069 | 0.591 |
MOD_PKB_1 | 280 | 288 | PF00069 | 0.597 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.476 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.413 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.337 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.369 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.644 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.563 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 56 | 61 | PF01217 | 0.604 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 107 | 110 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.552 |
TRG_NLS_MonoCore_2 | 96 | 101 | PF00514 | 0.544 |
TRG_NLS_MonoExtC_3 | 96 | 102 | PF00514 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHA6 | Leptomonas seymouri | 57% | 100% |
A0A1X0NNF4 | Trypanosomatidae | 28% | 90% |
A0A3S7WT74 | Leishmania donovani | 90% | 100% |
A0A422NFP0 | Trypanosoma rangeli | 34% | 100% |
A4H7V1 | Leishmania braziliensis | 81% | 100% |
A4HW77 | Leishmania infantum | 91% | 100% |
C9ZST9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4QFK3 | Leishmania major | 92% | 100% |
V5AW09 | Trypanosoma cruzi | 36% | 100% |