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: A4HU59
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 235 | 239 | PF00656 | 0.823 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.830 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.766 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.547 |
CLV_PCSK_PC1ET2_1 | 229 | 231 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.596 |
CLV_PCSK_PC7_1 | 225 | 231 | PF00082 | 0.675 |
CLV_PCSK_PC7_1 | 244 | 250 | PF00082 | 0.726 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.414 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.674 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.800 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.642 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.782 |
LIG_14-3-3_CanoR_1 | 111 | 116 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 138 | 144 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 215 | 219 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 230 | 235 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 248 | 257 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 68 | 76 | PF00244 | 0.566 |
LIG_Actin_WH2_2 | 217 | 234 | PF00022 | 0.673 |
LIG_BIR_III_2 | 41 | 45 | PF00653 | 0.591 |
LIG_CaM_IQ_9 | 95 | 111 | PF13499 | 0.506 |
LIG_Clathr_ClatBox_1 | 112 | 116 | PF01394 | 0.623 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.408 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.545 |
LIG_LIR_Apic_2 | 191 | 196 | PF02991 | 0.801 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.795 |
LIG_SH2_NCK_1 | 193 | 197 | PF00017 | 0.678 |
LIG_SH3_1 | 9 | 15 | PF00018 | 0.690 |
LIG_SH3_2 | 44 | 49 | PF14604 | 0.591 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.621 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.705 |
LIG_SUMO_SIM_par_1 | 111 | 118 | PF11976 | 0.625 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.626 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.660 |
MOD_CDC14_SPxK_1 | 11 | 14 | PF00782 | 0.637 |
MOD_CDK_SPK_2 | 175 | 180 | PF00069 | 0.661 |
MOD_CDK_SPK_2 | 239 | 244 | PF00069 | 0.641 |
MOD_CDK_SPxK_1 | 184 | 190 | PF00069 | 0.639 |
MOD_CDK_SPxK_1 | 8 | 14 | PF00069 | 0.632 |
MOD_CDK_SPxxK_3 | 192 | 199 | PF00069 | 0.700 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.717 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.466 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.662 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.618 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.593 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.547 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.678 |
MOD_Cter_Amidation | 199 | 202 | PF01082 | 0.592 |
MOD_Cter_Amidation | 50 | 53 | PF01082 | 0.593 |
MOD_GlcNHglycan | 116 | 120 | PF01048 | 0.629 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.647 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.694 |
MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.687 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.684 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.604 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.547 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.760 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.720 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.479 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.710 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.707 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.497 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.589 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.539 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.517 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.802 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.808 |
MOD_PK_1 | 230 | 236 | PF00069 | 0.707 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.762 |
MOD_PKA_1 | 248 | 254 | PF00069 | 0.819 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.675 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.709 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.678 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.669 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.724 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.569 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.675 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.677 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.679 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.724 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.709 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.784 |
MOD_SUMO_rev_2 | 94 | 104 | PF00179 | 0.413 |
TRG_DiLeu_BaEn_4 | 159 | 165 | PF01217 | 0.533 |
TRG_DiLeu_BaLyEn_6 | 35 | 40 | PF01217 | 0.760 |
TRG_Pf-PMV_PEXEL_1 | 82 | 87 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8A2 | Leptomonas seymouri | 44% | 97% |
A0A3S5H6E8 | Leishmania donovani | 100% | 100% |
A4H5W4 | Leishmania braziliensis | 69% | 100% |
E9AMY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QHN8 | Leishmania major | 91% | 100% |