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: A4HGF0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.800 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.803 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.794 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.727 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.810 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.731 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.610 |
CLV_PCSK_PC7_1 | 15 | 21 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.522 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.666 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.809 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.491 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.820 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 317 | 326 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 53 | 61 | PF00244 | 0.552 |
LIG_APCC_ABBA_1 | 148 | 153 | PF00400 | 0.512 |
LIG_APCC_ABBAyCdc20_2 | 147 | 153 | PF00400 | 0.513 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.824 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.768 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.655 |
LIG_HCF-1_HBM_1 | 303 | 306 | PF13415 | 0.532 |
LIG_Integrin_isoDGR_2 | 315 | 317 | PF01839 | 0.545 |
LIG_Integrin_RGD_1 | 272 | 274 | PF01839 | 0.593 |
LIG_LIR_Gen_1 | 153 | 163 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.537 |
LIG_SH2_GRB2like | 306 | 309 | PF00017 | 0.719 |
LIG_SH2_SRC | 335 | 338 | PF00017 | 0.669 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 394 | 398 | PF00017 | 0.813 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.691 |
LIG_SH3_1 | 42 | 48 | PF00018 | 0.548 |
LIG_SH3_2 | 188 | 193 | PF14604 | 0.574 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.567 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.575 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.762 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.561 |
MOD_CDK_SPxxK_3 | 102 | 109 | PF00069 | 0.558 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.575 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.577 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.804 |
MOD_Cter_Amidation | 171 | 174 | PF01082 | 0.571 |
MOD_Cter_Amidation | 204 | 207 | PF01082 | 0.815 |
MOD_Cter_Amidation | 22 | 25 | PF01082 | 0.641 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.812 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.728 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.613 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.804 |
MOD_GlcNHglycan | 225 | 229 | PF01048 | 0.795 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.570 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.702 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.739 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.567 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.775 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.629 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.679 |
MOD_N-GLC_2 | 219 | 221 | PF02516 | 0.586 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.702 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.652 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.572 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.635 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.670 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.642 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.761 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.819 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.559 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.815 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.831 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P454 | Leptomonas seymouri | 38% | 100% |
A0A3S7X1G1 | Leishmania donovani | 61% | 100% |
A4I3I1 | Leishmania infantum | 61% | 100% |
E9AZS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
Q4Q8G1 | Leishmania major | 62% | 100% |