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: A4HQG4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.546 |
DEG_APCC_DBOX_1 | 54 | 62 | PF00400 | 0.361 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.442 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.513 |
DEG_SPOP_SBC_1 | 250 | 254 | PF00917 | 0.608 |
DOC_MAPK_gen_1 | 215 | 221 | PF00069 | 0.594 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.524 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.515 |
DOC_USP7_UBL2_3 | 44 | 48 | PF12436 | 0.529 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 249 | 259 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 264 | 271 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 55 | 59 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 80 | 84 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 99 | 109 | PF00244 | 0.599 |
LIG_CaM_NSCaTE_8 | 129 | 136 | PF13499 | 0.313 |
LIG_deltaCOP1_diTrp_1 | 117 | 125 | PF00928 | 0.557 |
LIG_EH1_1 | 59 | 67 | PF00400 | 0.476 |
LIG_eIF4E_1 | 60 | 66 | PF01652 | 0.435 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.569 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.567 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.456 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.616 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.599 |
LIG_GBD_Chelix_1 | 58 | 66 | PF00786 | 0.503 |
LIG_LIR_Gen_1 | 25 | 34 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 25 | 29 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 305 | 310 | PF02991 | 0.450 |
LIG_Pex14_2 | 125 | 129 | PF04695 | 0.415 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.594 |
LIG_SH2_SRC | 60 | 63 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.431 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.675 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.351 |
LIG_UBA3_1 | 109 | 114 | PF00899 | 0.543 |
LIG_UBA3_1 | 218 | 223 | PF00899 | 0.593 |
LIG_WRC_WIRS_1 | 303 | 308 | PF05994 | 0.663 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.567 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.628 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.696 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.606 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.600 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.335 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.592 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.576 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.714 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.726 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.694 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.710 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.727 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.552 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.450 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.620 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.721 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.720 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.665 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.614 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.743 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.546 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.393 |
MOD_PKA_1 | 79 | 85 | PF00069 | 0.443 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.578 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.680 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.594 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.475 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.466 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.567 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.666 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.470 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.613 |
MOD_SUMO_for_1 | 282 | 285 | PF00179 | 0.800 |
MOD_SUMO_for_1 | 296 | 299 | PF00179 | 0.531 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.570 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IY70 | Bodo saltans | 29% | 100% |
A0A1X0NLM3 | Trypanosomatidae | 32% | 100% |
A0A3Q8IGT5 | Leishmania donovani | 85% | 100% |
A0A3R7NPS1 | Trypanosoma rangeli | 34% | 100% |
A4ICA0 | Leishmania infantum | 86% | 100% |
D0A3L5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AU80 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q0B4 | Leishmania major | 85% | 100% |
V5D8U2 | Trypanosoma cruzi | 34% | 100% |