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: 30 |
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: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 2, no: 23 |
NetGPI | no | yes: 0, no: 25 |
Related structures:
AlphaFold database: E9AMB0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 199 | 203 | PF00656 | 0.410 |
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.454 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.219 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.487 |
CLV_PCSK_FUR_1 | 230 | 234 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.548 |
DOC_ANK_TNKS_1 | 232 | 239 | PF00023 | 0.488 |
DOC_MAPK_gen_1 | 154 | 162 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 204 | 212 | PF00069 | 0.485 |
DOC_MAPK_MEF2A_6 | 154 | 162 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 204 | 212 | PF00069 | 0.373 |
DOC_PP2B_PxIxI_1 | 207 | 213 | PF00149 | 0.293 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.445 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.477 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 16 | 21 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 221 | 225 | PF00244 | 0.331 |
LIG_Actin_WH2_2 | 191 | 209 | PF00022 | 0.232 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.384 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.496 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.573 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.503 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.567 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.507 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.381 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.371 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 258 | 269 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.391 |
LIG_Pex14_2 | 216 | 220 | PF04695 | 0.311 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.389 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.313 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.298 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.389 |
LIG_SH3_1 | 9 | 15 | PF00018 | 0.467 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.443 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.327 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.733 |
LIG_SH3_4 | 207 | 214 | PF00018 | 0.372 |
LIG_TYR_ITIM | 39 | 44 | PF00017 | 0.265 |
LIG_UBA3_1 | 209 | 215 | PF00899 | 0.537 |
LIG_WW_3 | 13 | 17 | PF00397 | 0.445 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.517 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.572 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.395 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.475 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.569 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.577 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.667 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.357 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.384 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.403 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.502 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.503 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.371 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.321 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.424 |
MOD_OFUCOSY | 136 | 141 | PF10250 | 0.161 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.497 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.494 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.493 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.548 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.483 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.316 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.488 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.418 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.412 |
TRG_DiLeu_BaEn_1 | 22 | 27 | PF01217 | 0.391 |
TRG_DiLeu_LyEn_5 | 22 | 27 | PF01217 | 0.391 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.300 |
TRG_NES_CRM1_1 | 150 | 163 | PF08389 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P932 | Leptomonas seymouri | 37% | 100% |
A0A0N1HWD2 | Leptomonas seymouri | 31% | 100% |
A0A0N1I400 | Leptomonas seymouri | 54% | 100% |
A0A0N1IAK4 | Leptomonas seymouri | 41% | 100% |
A0A3S5H641 | Leishmania donovani | 37% | 100% |
A0A3S5H642 | Leishmania donovani | 46% | 100% |
A0A3S5IQS6 | Trypanosoma rangeli | 37% | 100% |
A0A3S7WQ71 | Leishmania donovani | 83% | 89% |
A4H5A0 | Leishmania braziliensis | 40% | 100% |
A4H5A1 | Leishmania braziliensis | 68% | 100% |
A4H5A2 | Leishmania braziliensis | 46% | 100% |
A4H6S1 | Leishmania braziliensis | 33% | 98% |
A4HTI1 | Leishmania infantum | 37% | 100% |
A4HTI2 | Leishmania infantum | 83% | 89% |
A4HTI3 | Leishmania infantum | 46% | 100% |
A4HV50 | Leishmania infantum | 30% | 100% |
D0VWV0 | Leishmania donovani | 30% | 100% |
E9AMA9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AMB1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9ANT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
P85094 | Mus musculus | 30% | 100% |
Q08C33 | Danio rerio | 25% | 97% |
Q4QGT7 | Leishmania major | 31% | 98% |
Q4QID7 | Leishmania major | 46% | 100% |
Q4QID8 | Leishmania major | 81% | 100% |
Q4QID9 | Leishmania major | 38% | 100% |