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: A4ICA0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.546 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.453 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.266 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.501 |
DEG_APCC_DBOX_1 | 54 | 62 | PF00400 | 0.482 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.496 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.502 |
DOC_MAPK_gen_1 | 215 | 221 | PF00069 | 0.582 |
DOC_PP1_SILK_1 | 80 | 85 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.564 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.547 |
DOC_USP7_UBL2_3 | 44 | 48 | PF12436 | 0.558 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.783 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 249 | 259 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 55 | 59 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 99 | 109 | PF00244 | 0.591 |
LIG_deltaCOP1_diTrp_1 | 117 | 125 | PF00928 | 0.586 |
LIG_EH1_1 | 59 | 67 | PF00400 | 0.562 |
LIG_eIF4E_1 | 60 | 66 | PF01652 | 0.534 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.589 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.480 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.586 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.585 |
LIG_GBD_Chelix_1 | 58 | 66 | PF00786 | 0.386 |
LIG_LIR_Gen_1 | 116 | 127 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 25 | 34 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 25 | 29 | PF02991 | 0.534 |
LIG_Pex14_2 | 125 | 129 | PF04695 | 0.482 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.582 |
LIG_SH2_SRC | 60 | 63 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.533 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.747 |
LIG_UBA3_1 | 109 | 114 | PF00899 | 0.586 |
LIG_UBA3_1 | 218 | 223 | PF00899 | 0.582 |
LIG_WRC_WIRS_1 | 303 | 308 | PF05994 | 0.698 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.586 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.566 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.720 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.775 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.581 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.585 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.604 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.572 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.698 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.732 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.489 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.736 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.685 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.726 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.386 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.494 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.624 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.722 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.637 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.803 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.591 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.536 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.480 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.715 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.565 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.671 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.740 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.561 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.586 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.698 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.557 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.606 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.779 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.591 |
MOD_SUMO_for_1 | 282 | 285 | PF00179 | 0.774 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IY70 | Bodo saltans | 28% | 100% |
A0A1X0NLM3 | Trypanosomatidae | 33% | 100% |
A0A3Q8IGT5 | Leishmania donovani | 99% | 100% |
A0A3R7NPS1 | Trypanosoma rangeli | 37% | 100% |
A4HQG4 | Leishmania braziliensis | 86% | 100% |
D0A3L5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AU80 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q0B4 | Leishmania major | 94% | 100% |
V5D8U2 | Trypanosoma cruzi | 34% | 100% |