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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AUR5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 182 | 184 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.545 |
DOC_CKS1_1 | 40 | 45 | PF01111 | 0.526 |
DOC_SPAK_OSR1_1 | 141 | 145 | PF12202 | 0.609 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.655 |
DOC_USP7_MATH_2 | 235 | 241 | PF00917 | 0.296 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.706 |
LIG_14-3-3_CanoR_1 | 198 | 205 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.220 |
LIG_APCC_ABBA_1 | 54 | 59 | PF00400 | 0.488 |
LIG_BIR_III_2 | 254 | 258 | PF00653 | 0.437 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.405 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.611 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.541 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.275 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.516 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.500 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.654 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.576 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.356 |
LIG_HCF-1_HBM_1 | 162 | 165 | PF13415 | 0.296 |
LIG_LIR_Apic_2 | 147 | 153 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 245 | 249 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 55 | 60 | PF02991 | 0.486 |
LIG_LYPXL_S_1 | 56 | 60 | PF13949 | 0.487 |
LIG_PCNA_yPIPBox_3 | 166 | 179 | PF02747 | 0.405 |
LIG_PDZ_Class_2 | 261 | 266 | PF00595 | 0.573 |
LIG_SH2_PTP2 | 150 | 153 | PF00017 | 0.474 |
LIG_SH2_STAT3 | 64 | 67 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.356 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.690 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.528 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.710 |
LIG_SUMO_SIM_anti_2 | 99 | 107 | PF11976 | 0.591 |
LIG_UBA3_1 | 174 | 182 | PF00899 | 0.405 |
MOD_CDK_SPK_2 | 106 | 111 | PF00069 | 0.530 |
MOD_CDK_SPxxK_3 | 104 | 111 | PF00069 | 0.531 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.660 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.686 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.747 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.754 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.296 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.577 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.278 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.519 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.644 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.612 |
MOD_GlcNHglycan | 92 | 96 | PF01048 | 0.700 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.296 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.783 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.535 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.740 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.725 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.675 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.543 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.405 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.441 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.365 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.574 |
MOD_NEK2_2 | 205 | 210 | PF00069 | 0.477 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.405 |
MOD_NEK2_2 | 5 | 10 | PF00069 | 0.489 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.555 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.621 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.405 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.405 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.692 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.322 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.598 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.308 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.487 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.617 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.581 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.513 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.760 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.706 |
MOD_SPalmitoyl_4 | 1 | 7 | PF01529 | 0.555 |
TRG_DiLeu_BaEn_2 | 236 | 242 | PF01217 | 0.405 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IEW9 | Leishmania donovani | 79% | 100% |
A4HYW8 | Leishmania infantum | 79% | 100% |
E9AII0 | Leishmania braziliensis | 45% | 100% |
Q4QCS1 | Leishmania major | 75% | 100% |