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: A4H441
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.562 |
DEG_SCF_TRCP1_1 | 25 | 31 | PF00400 | 0.468 |
DEG_SPOP_SBC_1 | 265 | 269 | PF00917 | 0.572 |
DOC_PP1_RVXF_1 | 40 | 47 | PF00149 | 0.370 |
DOC_PP2B_LxvP_1 | 124 | 127 | PF13499 | 0.665 |
DOC_PP4_FxxP_1 | 46 | 49 | PF00568 | 0.408 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.759 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 115 | 124 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 129 | 133 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 16 | 24 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 218 | 226 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 322 | 330 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 68 | 78 | PF00244 | 0.418 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.517 |
LIG_BIR_III_4 | 258 | 262 | PF00653 | 0.536 |
LIG_CtBP_PxDLS_1 | 261 | 266 | PF00389 | 0.538 |
LIG_deltaCOP1_diTrp_1 | 164 | 169 | PF00928 | 0.550 |
LIG_deltaCOP1_diTrp_1 | 97 | 105 | PF00928 | 0.409 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.579 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.434 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.612 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.619 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.481 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.520 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.484 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.363 |
LIG_LIR_Apic_2 | 45 | 49 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 31 | 35 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.522 |
LIG_PCNA_PIPBox_1 | 188 | 197 | PF02747 | 0.427 |
LIG_SH2_STAT3 | 303 | 306 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 51 | 54 | PF00017 | 0.404 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.663 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.651 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.727 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.671 |
MOD_CDK_SPK_2 | 17 | 22 | PF00069 | 0.427 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.618 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.452 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.616 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.700 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.571 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.521 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.634 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.518 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.370 |
MOD_Cter_Amidation | 216 | 219 | PF01082 | 0.532 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.588 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.630 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.599 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.534 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.731 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.624 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.605 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.662 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.588 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.625 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.622 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.729 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.606 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.713 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.504 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.511 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.685 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.548 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.409 |
MOD_NEK2_2 | 167 | 172 | PF00069 | 0.373 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.603 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.473 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.550 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.584 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.395 |
MOD_PKA_1 | 218 | 224 | PF00069 | 0.579 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.593 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.416 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.599 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.626 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.539 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.716 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.535 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.504 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.521 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.435 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.588 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.536 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.662 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.461 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.469 |
TRG_PTS1 | 336 | 339 | PF00515 | 0.724 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P325 | Leptomonas seymouri | 30% | 96% |
A0A3S5H5B7 | Leishmania donovani | 58% | 100% |
A4HS58 | Leishmania infantum | 58% | 100% |
E9ACP8 | Leishmania major | 54% | 100% |
E9AK45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |