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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4IBS0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 284 | 290 | PF00089 | 0.339 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.645 |
CLV_PCSK_FUR_1 | 20 | 24 | PF00082 | 0.536 |
CLV_PCSK_FUR_1 | 269 | 273 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.442 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 271 | 273 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.523 |
CLV_PCSK_PC7_1 | 18 | 24 | PF00082 | 0.488 |
CLV_PCSK_PC7_1 | 267 | 273 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.480 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.441 |
DOC_CDC14_PxL_1 | 29 | 37 | PF14671 | 0.517 |
DOC_CKS1_1 | 160 | 165 | PF01111 | 0.546 |
DOC_CYCLIN_RxL_1 | 108 | 121 | PF00134 | 0.426 |
DOC_MAPK_gen_1 | 108 | 117 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 267 | 276 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 297 | 307 | PF00069 | 0.551 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.451 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.464 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 201 | 211 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 282 | 291 | PF00244 | 0.514 |
LIG_Actin_WH2_2 | 102 | 120 | PF00022 | 0.512 |
LIG_Actin_WH2_2 | 130 | 145 | PF00022 | 0.407 |
LIG_Actin_WH2_2 | 292 | 308 | PF00022 | 0.534 |
LIG_APCC_ABBAyCdc20_2 | 255 | 261 | PF00400 | 0.497 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.477 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.502 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.584 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.478 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.608 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.511 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.498 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.691 |
LIG_Integrin_RGD_1 | 244 | 246 | PF01839 | 0.484 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.536 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.505 |
LIG_SH2_SRC | 138 | 141 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.383 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.550 |
LIG_SUMO_SIM_anti_2 | 208 | 216 | PF11976 | 0.476 |
LIG_TRAF2_1 | 206 | 209 | PF00917 | 0.416 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.663 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.703 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.553 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.502 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.679 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.730 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.492 |
MOD_GlcNHglycan | 234 | 238 | PF01048 | 0.700 |
MOD_GlcNHglycan | 246 | 251 | PF01048 | 0.519 |
MOD_GlcNHglycan | 301 | 305 | PF01048 | 0.431 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.468 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.667 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.637 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.508 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.550 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.396 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.456 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.591 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.555 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.513 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.431 |
MOD_NEK2_2 | 138 | 143 | PF00069 | 0.430 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.538 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.583 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.548 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.613 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.409 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.470 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.426 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.621 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.581 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.571 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.415 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.479 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.554 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.592 |
TRG_DiLeu_BaEn_1 | 209 | 214 | PF01217 | 0.479 |
TRG_DiLeu_BaEn_4 | 97 | 103 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 279 | 284 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.508 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 100 | 105 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 282 | 286 | PF00026 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3I4 | Leptomonas seymouri | 35% | 93% |
A0A1X0P5H2 | Trypanosomatidae | 25% | 89% |
A0A3Q8IIM5 | Leishmania donovani | 100% | 100% |
A0A3R7NA43 | Trypanosoma rangeli | 29% | 88% |
A4HN53 | Leishmania braziliensis | 75% | 100% |
E9AFK6 | Leishmania major | 92% | 100% |
E9B6R0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5C2S8 | Trypanosoma cruzi | 29% | 88% |