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: A4HC00
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 104 | 108 | PF00656 | 0.523 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.730 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.581 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.510 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.667 |
DOC_USP7_UBL2_3 | 224 | 228 | PF12436 | 0.515 |
DOC_USP7_UBL2_3 | 250 | 254 | PF12436 | 0.557 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 160 | 165 | PF00244 | 0.392 |
LIG_14-3-3_CanoR_1 | 168 | 175 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 195 | 204 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 265 | 274 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 42 | 50 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 82 | 91 | PF00244 | 0.374 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.515 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.410 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.501 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.390 |
LIG_LIR_Apic_2 | 202 | 207 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 138 | 144 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 240 | 249 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 88 | 98 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.406 |
LIG_PTAP_UEV_1 | 291 | 296 | PF05743 | 0.563 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.502 |
LIG_SH2_NCK_1 | 275 | 279 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 150 | 154 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.437 |
LIG_SH3_1 | 211 | 217 | PF00018 | 0.503 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.675 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.570 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.515 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.583 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.361 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.572 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.562 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.491 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.479 |
MOD_CK2_1 | 253 | 259 | PF00069 | 0.478 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.426 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.472 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.443 |
MOD_Cter_Amidation | 25 | 28 | PF01082 | 0.577 |
MOD_Cter_Amidation | 250 | 253 | PF01082 | 0.556 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.432 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.730 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.444 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.467 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.739 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.624 |
MOD_GlcNHglycan | 60 | 64 | PF01048 | 0.630 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.376 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.469 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.550 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.614 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.533 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.613 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.713 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.474 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.448 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.352 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.593 |
MOD_PKA_1 | 253 | 259 | PF00069 | 0.374 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.432 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.488 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.501 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.371 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.489 |
MOD_PKB_1 | 166 | 174 | PF00069 | 0.411 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.642 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.505 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.487 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.536 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.583 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.477 |
MOD_SUMO_rev_2 | 268 | 274 | PF00179 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.498 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.287 |
TRG_Pf-PMV_PEXEL_1 | 211 | 215 | PF00026 | 0.566 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAX4 | Leptomonas seymouri | 31% | 99% |
A0A3Q8IL79 | Leishmania donovani | 60% | 100% |
A4HZE9 | Leishmania infantum | 60% | 100% |
E9AVD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
Q4QC43 | Leishmania major | 60% | 100% |