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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3Q8IF51
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.503 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.448 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.434 |
CLV_Separin_Metazoa | 178 | 182 | PF03568 | 0.552 |
DEG_APCC_DBOX_1 | 30 | 38 | PF00400 | 0.458 |
DEG_APCC_DBOX_1 | 99 | 107 | PF00400 | 0.409 |
DEG_SCF_FBW7_1 | 60 | 67 | PF00400 | 0.635 |
DOC_CKS1_1 | 61 | 66 | PF01111 | 0.639 |
DOC_CYCLIN_yCln2_LP_2 | 58 | 61 | PF00134 | 0.561 |
DOC_MAPK_gen_1 | 158 | 166 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 160 | 168 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 189 | 197 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 27 | 36 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 86 | 94 | PF00069 | 0.409 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.578 |
DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.757 |
DOC_PP2B_LxvP_1 | 58 | 61 | PF13499 | 0.609 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.654 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 114 | 118 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 15 | 23 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 31 | 37 | PF00244 | 0.449 |
LIG_Actin_WH2_2 | 165 | 183 | PF00022 | 0.476 |
LIG_Actin_WH2_2 | 87 | 102 | PF00022 | 0.436 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.460 |
LIG_FHA_2 | 173 | 179 | PF00498 | 0.488 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.625 |
LIG_GBD_Chelix_1 | 140 | 148 | PF00786 | 0.502 |
LIG_GSK3_LRP6_1 | 60 | 65 | PF00069 | 0.628 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 134 | 144 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 35 | 42 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.461 |
LIG_LYPXL_yS_3 | 87 | 90 | PF13949 | 0.417 |
LIG_OCRL_FandH_1 | 117 | 129 | PF00620 | 0.436 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.531 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.594 |
LIG_SUMO_SIM_anti_2 | 127 | 132 | PF11976 | 0.419 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.525 |
MOD_CDK_SPK_2 | 10 | 15 | PF00069 | 0.687 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.604 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.687 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.488 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.542 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.468 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.667 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.447 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.419 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.517 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.721 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.443 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.696 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.561 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.491 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.687 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.675 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.479 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.477 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.647 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.541 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.458 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.732 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.531 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.463 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.559 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.585 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.792 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.669 |
TRG_DiLeu_BaEn_1 | 89 | 94 | PF01217 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 29 | 34 | PF01217 | 0.586 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.417 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Z8 | Leptomonas seymouri | 65% | 91% |
A0A1X0P230 | Trypanosomatidae | 29% | 100% |
A0A3R7N1I2 | Trypanosoma rangeli | 30% | 100% |
A4HIN2 | Leishmania braziliensis | 77% | 100% |
A4I5X9 | Leishmania infantum | 100% | 100% |
C9ZRA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4Q6Z2 | Leishmania major | 92% | 100% |