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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q2F8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.489 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.582 |
DOC_CYCLIN_RxL_1 | 90 | 99 | PF00134 | 0.606 |
DOC_MAPK_gen_1 | 26 | 34 | PF00069 | 0.467 |
DOC_PP2B_LxvP_1 | 185 | 188 | PF13499 | 0.510 |
DOC_PP4_FxxP_1 | 152 | 155 | PF00568 | 0.507 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.487 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.757 |
LIG_14-3-3_CanoR_1 | 135 | 141 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.461 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.701 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.532 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.401 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.481 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.475 |
LIG_FHA_2 | 211 | 217 | PF00498 | 0.565 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.562 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.546 |
LIG_LIR_Gen_1 | 156 | 167 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 183 | 190 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 59 | 66 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 183 | 187 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.581 |
LIG_MLH1_MIPbox_1 | 190 | 194 | PF16413 | 0.487 |
LIG_NRBOX | 108 | 114 | PF00104 | 0.480 |
LIG_NRBOX | 206 | 212 | PF00104 | 0.478 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.639 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.563 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.650 |
LIG_SUMO_SIM_anti_2 | 30 | 36 | PF11976 | 0.563 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.518 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.736 |
LIG_WRC_WIRS_1 | 161 | 166 | PF05994 | 0.337 |
MOD_CDK_SPK_2 | 4 | 9 | PF00069 | 0.641 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.699 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.600 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.529 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.776 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.433 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.532 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.754 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.520 |
MOD_CMANNOS | 181 | 184 | PF00535 | 0.389 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.470 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.747 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.557 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.616 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.530 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.525 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.445 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.635 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.560 |
MOD_N-GLC_2 | 176 | 178 | PF02516 | 0.465 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.478 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.494 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.543 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.437 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.612 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.601 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.451 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.672 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.628 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.547 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.563 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.422 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.411 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.523 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.574 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.601 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.754 |
MOD_SUMO_rev_2 | 59 | 67 | PF00179 | 0.570 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.384 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE51 | Leptomonas seymouri | 54% | 98% |
A0A0S4KKN8 | Bodo saltans | 28% | 92% |
A0A1X0ND66 | Trypanosomatidae | 34% | 100% |
A0A3Q8IEP6 | Leishmania donovani | 86% | 100% |
A0A422NSY2 | Trypanosoma rangeli | 36% | 100% |
A4HBA5 | Leishmania braziliensis | 66% | 96% |
A4IAF3 | Leishmania infantum | 86% | 100% |
C9ZLU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B5H7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |