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: A4H6C7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.646 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.503 |
DEG_SCF_TRCP1_1 | 175 | 180 | PF00400 | 0.570 |
DEG_SIAH_1 | 309 | 317 | PF03145 | 0.460 |
DOC_CYCLIN_yCln2_LP_2 | 209 | 215 | PF00134 | 0.529 |
DOC_MAPK_MEF2A_6 | 221 | 229 | PF00069 | 0.558 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.571 |
DOC_PP4_MxPP_1 | 223 | 226 | PF00568 | 0.718 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.587 |
DOC_USP7_UBL2_3 | 147 | 151 | PF12436 | 0.673 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.618 |
LIG_AP2alpha_1 | 229 | 233 | PF02296 | 0.738 |
LIG_AP2alpha_1 | 273 | 277 | PF02296 | 0.477 |
LIG_AP2alpha_2 | 211 | 213 | PF02296 | 0.724 |
LIG_AP2alpha_2 | 231 | 233 | PF02296 | 0.562 |
LIG_AP2alpha_2 | 309 | 311 | PF02296 | 0.512 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.595 |
LIG_BIR_III_2 | 199 | 203 | PF00653 | 0.558 |
LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.534 |
LIG_EH_1 | 284 | 288 | PF12763 | 0.476 |
LIG_EVH1_2 | 225 | 229 | PF00568 | 0.726 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.557 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.570 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.577 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 308 | 316 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 85 | 96 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.487 |
LIG_Pex14_2 | 229 | 233 | PF04695 | 0.738 |
LIG_Pex14_2 | 273 | 277 | PF04695 | 0.548 |
LIG_Pex14_2 | 311 | 315 | PF04695 | 0.446 |
LIG_Pex14_2 | 69 | 73 | PF04695 | 0.662 |
LIG_SH2_GRB2like | 60 | 63 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 235 | 238 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.581 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.691 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.635 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.554 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.591 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.588 |
LIG_SUMO_SIM_par_1 | 119 | 126 | PF11976 | 0.775 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.578 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.578 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.780 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.564 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.523 |
MOD_Cter_Amidation | 184 | 187 | PF01082 | 0.783 |
MOD_Cter_Amidation | 244 | 247 | PF01082 | 0.577 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.649 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.670 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.684 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.637 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.582 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.697 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.583 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.583 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.508 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.584 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.519 |
MOD_LATS_1 | 3 | 9 | PF00433 | 0.560 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.559 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.615 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.518 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.572 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.548 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.652 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.567 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.539 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.637 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.690 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.560 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.614 |
TRG_ER_diArg_1 | 105 | 108 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.646 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEG2 | Leptomonas seymouri | 37% | 100% |
A0A3S5H670 | Leishmania donovani | 58% | 100% |
A4HTM6 | Leishmania infantum | 58% | 100% |
E9AMG0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
Q4QI83 | Leishmania major | 58% | 93% |