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: A0A3Q8IDH2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.585 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.549 |
DEG_SPOP_SBC_1 | 184 | 188 | PF00917 | 0.712 |
DOC_CKS1_1 | 14 | 19 | PF01111 | 0.672 |
DOC_CYCLIN_RxL_1 | 62 | 72 | PF00134 | 0.577 |
DOC_PP2B_LxvP_1 | 228 | 231 | PF13499 | 0.491 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.569 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 166 | 170 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.533 |
LIG_BRCT_BRCA1_1 | 287 | 291 | PF00533 | 0.588 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.754 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.684 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.598 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.761 |
LIG_Integrin_RGD_1 | 279 | 281 | PF01839 | 0.692 |
LIG_MYND_1 | 118 | 122 | PF01753 | 0.692 |
LIG_RPA_C_Fungi | 208 | 220 | PF08784 | 0.548 |
LIG_RPA_C_Fungi | 48 | 60 | PF08784 | 0.537 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.610 |
LIG_SH3_1 | 11 | 17 | PF00018 | 0.610 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.634 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.616 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.712 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.627 |
LIG_SUMO_SIM_par_1 | 204 | 210 | PF11976 | 0.542 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.602 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.738 |
LIG_WW_2 | 17 | 20 | PF00397 | 0.678 |
LIG_WW_3 | 196 | 200 | PF00397 | 0.703 |
MOD_CDK_SPxxK_3 | 2 | 9 | PF00069 | 0.698 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.707 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.615 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.659 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.754 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.705 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.614 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.658 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.563 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.574 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.561 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.605 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.402 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.601 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.742 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.595 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.495 |
MOD_GlcNHglycan | 177 | 181 | PF01048 | 0.662 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.822 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.625 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.616 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.650 |
MOD_GlcNHglycan | 263 | 268 | PF01048 | 0.698 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.719 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.751 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.730 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.764 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.476 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.622 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.704 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.515 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.556 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.654 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.513 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.744 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.552 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.549 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.591 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.518 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.492 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.749 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.762 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.756 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.601 |
TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.376 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC2 | Leptomonas seymouri | 40% | 88% |
A4H899 | Leishmania braziliensis | 62% | 100% |
A4HWM1 | Leishmania infantum | 100% | 100% |
E9AQC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QF47 | Leishmania major | 89% | 100% |