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: A4HJR8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.493 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.522 |
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.562 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 104 | 108 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.504 |
CLV_Separin_Metazoa | 179 | 183 | PF03568 | 0.635 |
DOC_MAPK_gen_1 | 116 | 123 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 182 | 190 | PF00069 | 0.560 |
DOC_PP1_RVXF_1 | 62 | 68 | PF00149 | 0.537 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.545 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.513 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.537 |
LIG_14-3-3_CanoR_1 | 107 | 113 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 149 | 158 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 182 | 192 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.583 |
LIG_APCC_ABBA_1 | 200 | 205 | PF00400 | 0.690 |
LIG_BRCT_BRCA1_1 | 238 | 242 | PF00533 | 0.475 |
LIG_CAP-Gly_1 | 244 | 248 | PF01302 | 0.479 |
LIG_CSL_BTD_1 | 21 | 24 | PF09270 | 0.499 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.497 |
LIG_LIR_Gen_1 | 66 | 75 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 119 | 123 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.532 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.686 |
LIG_SH2_GRB2like | 145 | 148 | PF00017 | 0.513 |
LIG_SH2_PTP2 | 120 | 123 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.475 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.535 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.702 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.530 |
MOD_CDC14_SPxK_1 | 30 | 33 | PF00782 | 0.592 |
MOD_CDK_SPK_2 | 154 | 159 | PF00069 | 0.517 |
MOD_CDK_SPK_2 | 27 | 32 | PF00069 | 0.534 |
MOD_CDK_SPxK_1 | 154 | 160 | PF00069 | 0.516 |
MOD_CDK_SPxK_1 | 27 | 33 | PF00069 | 0.592 |
MOD_CDK_SPxxK_3 | 44 | 51 | PF00069 | 0.534 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.481 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.799 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.586 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.792 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.570 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.662 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.534 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.492 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.584 |
MOD_DYRK1A_RPxSP_1 | 27 | 31 | PF00069 | 0.530 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.471 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.548 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.769 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.677 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.628 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.565 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.811 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.515 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.694 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.572 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.559 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.676 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.566 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.542 |
MOD_PKA_1 | 159 | 165 | PF00069 | 0.500 |
MOD_PKA_1 | 182 | 188 | PF00069 | 0.543 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.520 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.500 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.543 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.633 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.580 |
MOD_Plk_2-3 | 63 | 69 | PF00069 | 0.539 |
MOD_Plk_2-3 | 93 | 99 | PF00069 | 0.632 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.572 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.492 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.563 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.548 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.530 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.571 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.510 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.539 |
MOD_SUMO_rev_2 | 124 | 130 | PF00179 | 0.586 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.566 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_3 | 237 | 243 | PF01217 | 0.665 |
TRG_DiLeu_BaEn_4 | 60 | 66 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.545 |
TRG_ER_diArg_1 | 104 | 107 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 33 | 37 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJH6 | Leptomonas seymouri | 40% | 98% |
A0A3Q8IF41 | Leishmania donovani | 55% | 92% |
E9AHL9 | Leishmania infantum | 54% | 92% |
E9B279 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 93% |
Q4Q5X9 | Leishmania major | 56% | 100% |