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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 16 |
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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4H5N3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.249 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.605 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.508 |
DEG_SCF_FBW7_1 | 303 | 310 | PF00400 | 0.376 |
DOC_CDC14_PxL_1 | 239 | 247 | PF14671 | 0.522 |
DOC_CKS1_1 | 304 | 309 | PF01111 | 0.535 |
DOC_CYCLIN_RxL_1 | 231 | 244 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 204 | 210 | PF00134 | 0.558 |
DOC_MAPK_MEF2A_6 | 144 | 152 | PF00069 | 0.511 |
DOC_MAPK_RevD_3 | 208 | 222 | PF00069 | 0.369 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.526 |
DOC_PP4_FxxP_1 | 181 | 184 | PF00568 | 0.520 |
DOC_PP4_FxxP_1 | 25 | 28 | PF00568 | 0.661 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.535 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.646 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.430 |
LIG_14-3-3_CanoR_1 | 123 | 132 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 275 | 284 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 64 | 71 | PF00244 | 0.501 |
LIG_Actin_WH2_2 | 108 | 125 | PF00022 | 0.476 |
LIG_AP2alpha_1 | 21 | 25 | PF02296 | 0.468 |
LIG_APCC_ABBA_1 | 148 | 153 | PF00400 | 0.418 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.476 |
LIG_EH_1 | 205 | 209 | PF12763 | 0.576 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.498 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.359 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.532 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.447 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.549 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.538 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.565 |
LIG_GBD_Chelix_1 | 95 | 103 | PF00786 | 0.430 |
LIG_LIR_Apic_2 | 178 | 184 | PF02991 | 0.511 |
LIG_LIR_Apic_2 | 22 | 28 | PF02991 | 0.641 |
LIG_LIR_Apic_2 | 302 | 307 | PF02991 | 0.559 |
LIG_LIR_Apic_2 | 44 | 50 | PF02991 | 0.472 |
LIG_LIR_Apic_2 | 79 | 83 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 281 | 289 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.459 |
LIG_Pex14_2 | 21 | 25 | PF04695 | 0.468 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.493 |
LIG_SH2_NCK_1 | 188 | 192 | PF00017 | 0.523 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.498 |
LIG_SH2_SRC | 151 | 154 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.452 |
LIG_SH3_2 | 226 | 231 | PF14604 | 0.337 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.538 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.562 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.409 |
LIG_SUMO_SIM_anti_2 | 110 | 116 | PF11976 | 0.449 |
LIG_SUMO_SIM_anti_2 | 249 | 254 | PF11976 | 0.556 |
LIG_SUMO_SIM_par_1 | 113 | 119 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 238 | 244 | PF11976 | 0.601 |
LIG_TRFH_1 | 208 | 212 | PF08558 | 0.497 |
MOD_CDK_SPxxK_3 | 116 | 123 | PF00069 | 0.376 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.476 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.456 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.430 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.614 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.555 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.593 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.550 |
MOD_GlcNHglycan | 289 | 293 | PF01048 | 0.597 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.422 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.457 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.567 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.538 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.435 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.416 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.469 |
MOD_N-GLC_1 | 275 | 280 | PF02516 | 0.486 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.500 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.354 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.457 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.434 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.430 |
MOD_NEK2_2 | 214 | 219 | PF00069 | 0.572 |
MOD_NEK2_2 | 256 | 261 | PF00069 | 0.324 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.363 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.501 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.579 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.417 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.430 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.323 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.398 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.612 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.538 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.376 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.505 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.430 |
MOD_SUMO_rev_2 | 244 | 250 | PF00179 | 0.586 |
MOD_SUMO_rev_2 | 310 | 316 | PF00179 | 0.461 |
TRG_DiLeu_BaLyEn_6 | 117 | 122 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.452 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.249 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4Q9 | Leptomonas seymouri | 57% | 100% |
A0A0S4JZY4 | Bodo saltans | 40% | 100% |
A0A3S7WQN5 | Leishmania donovani | 79% | 100% |
A4HTX7 | Leishmania infantum | 79% | 100% |
E9AMQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QHW8 | Leishmania major | 78% | 100% |