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: E9B1A7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.832 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.481 |
CLV_Separin_Metazoa | 114 | 118 | PF03568 | 0.489 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.489 |
DEG_COP1_1 | 255 | 265 | PF00400 | 0.516 |
DEG_COP1_1 | 71 | 79 | PF00400 | 0.547 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.646 |
DEG_SCF_FBW7_1 | 284 | 290 | PF00400 | 0.512 |
DOC_CDC14_PxL_1 | 73 | 81 | PF14671 | 0.546 |
DOC_CKS1_1 | 232 | 237 | PF01111 | 0.526 |
DOC_CKS1_1 | 248 | 253 | PF01111 | 0.556 |
DOC_CKS1_1 | 284 | 289 | PF01111 | 0.519 |
DOC_CKS1_1 | 310 | 315 | PF01111 | 0.664 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.531 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 177 | 185 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 199 | 208 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 39 | 47 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 9 | 18 | PF00244 | 0.566 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.589 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.491 |
LIG_CtBP_PxDLS_1 | 26 | 30 | PF00389 | 0.675 |
LIG_deltaCOP1_diTrp_1 | 169 | 176 | PF00928 | 0.507 |
LIG_eIF4E_1 | 283 | 289 | PF01652 | 0.609 |
LIG_EVH1_1 | 242 | 246 | PF00568 | 0.706 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.562 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.483 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.517 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.698 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.579 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.754 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.455 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.509 |
LIG_LIR_Apic_2 | 349 | 355 | PF02991 | 0.697 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 139 | 147 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 157 | 162 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 210 | 219 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 139 | 143 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 157 | 161 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.511 |
LIG_MYND_1 | 235 | 239 | PF01753 | 0.597 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.512 |
LIG_REV1ctd_RIR_1 | 140 | 150 | PF16727 | 0.499 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.480 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.505 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.699 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.707 |
LIG_SH2_CRK | 73 | 77 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 254 | 258 | PF00017 | 0.480 |
LIG_SH2_SRC | 252 | 255 | PF00017 | 0.774 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.707 |
LIG_SH2_SRC | 352 | 355 | PF00017 | 0.705 |
LIG_SH2_STAP1 | 252 | 256 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.509 |
LIG_SH3_1 | 74 | 80 | PF00018 | 0.548 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.553 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.590 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.604 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.642 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.632 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.725 |
LIG_SH3_3 | 291 | 297 | PF00018 | 0.658 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.548 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.515 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.573 |
LIG_TYR_ITSM | 310 | 317 | PF00017 | 0.502 |
LIG_WRC_WIRS_1 | 116 | 121 | PF05994 | 0.580 |
LIG_WRC_WIRS_1 | 208 | 213 | PF05994 | 0.491 |
MOD_CDC14_SPxK_1 | 153 | 156 | PF00782 | 0.599 |
MOD_CDK_SPxK_1 | 150 | 156 | PF00069 | 0.577 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.350 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.482 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.777 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.566 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.486 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.598 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.423 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.505 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.585 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.683 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.638 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.481 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.630 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.345 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.480 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.498 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.572 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.798 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.625 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.762 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.755 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.715 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.578 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.597 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.581 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.522 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.515 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.449 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.478 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.508 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.555 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.509 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.555 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.489 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.641 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.507 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.553 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.562 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.483 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.486 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.577 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.700 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.532 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.557 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.707 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.622 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.779 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.653 |
MOD_SUMO_for_1 | 43 | 46 | PF00179 | 0.329 |
MOD_SUMO_rev_2 | 68 | 76 | PF00179 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 284 | 289 | PF01217 | 0.616 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.507 |
TRG_NES_CRM1_1 | 85 | 99 | PF08389 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P436 | Leptomonas seymouri | 62% | 95% |
A0A3Q8IG34 | Leishmania donovani | 90% | 99% |
A4HIS0 | Leishmania braziliensis | 76% | 100% |
A4I616 | Leishmania infantum | 90% | 99% |
Q4Q6V7 | Leishmania major | 89% | 100% |