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: Q4QIS3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.632 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.668 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.709 |
DEG_SCF_FBW7_1 | 223 | 228 | PF00400 | 0.558 |
DEG_SCF_FBW7_1 | 84 | 91 | PF00400 | 0.742 |
DEG_SPOP_SBC_1 | 71 | 75 | PF00917 | 0.505 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.564 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.742 |
DOC_MAPK_MEF2A_6 | 138 | 146 | PF00069 | 0.558 |
DOC_PP2B_LxvP_1 | 186 | 189 | PF13499 | 0.662 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.801 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.654 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.816 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 36 | 43 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.419 |
LIG_APCC_ABBA_1 | 115 | 120 | PF00400 | 0.644 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.503 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.649 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.739 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.587 |
LIG_LIR_Apic_2 | 220 | 225 | PF02991 | 0.747 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 49 | 59 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.784 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.585 |
LIG_PAM2_1 | 49 | 61 | PF00658 | 0.430 |
LIG_PCNA_yPIPBox_3 | 177 | 186 | PF02747 | 0.533 |
LIG_PDZ_Class_1 | 249 | 254 | PF00595 | 0.705 |
LIG_Pex14_1 | 151 | 155 | PF04695 | 0.411 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.594 |
LIG_SH2_CRK | 60 | 64 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 162 | 166 | PF00017 | 0.650 |
LIG_SH2_NCK_1 | 60 | 64 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 242 | 246 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.416 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.712 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.690 |
LIG_TRAF2_1 | 39 | 42 | PF00917 | 0.588 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.720 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.701 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.550 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.661 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.828 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.703 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.660 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.668 |
MOD_GlcNHglycan | 226 | 230 | PF01048 | 0.661 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.711 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.555 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.689 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.548 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.564 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.740 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.786 |
MOD_LATS_1 | 211 | 217 | PF00433 | 0.697 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.579 |
MOD_N-GLC_1 | 214 | 219 | PF02516 | 0.759 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.551 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.619 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.640 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.575 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.396 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.559 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.558 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.578 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.687 |
MOD_Plk_1 | 231 | 237 | PF00069 | 0.718 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.516 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.634 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.547 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.716 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.610 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.725 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.633 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.585 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.711 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.816 |
MOD_SUMO_rev_2 | 133 | 140 | PF00179 | 0.657 |
TRG_DiLeu_BaLyEn_6 | 137 | 142 | PF01217 | 0.598 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.416 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I988 | Leptomonas seymouri | 37% | 100% |
A0A3S5H5W6 | Leishmania donovani | 89% | 100% |
A4H4W5 | Leishmania braziliensis | 60% | 100% |
A4HT39 | Leishmania infantum | 88% | 100% |
E9AL31 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |