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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B0X0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.795 |
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.650 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.667 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.686 |
CLV_PCSK_FUR_1 | 16 | 20 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.656 |
DEG_APCC_DBOX_1 | 238 | 246 | PF00400 | 0.408 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.702 |
DEG_SPOP_SBC_1 | 286 | 290 | PF00917 | 0.592 |
DOC_CKS1_1 | 98 | 103 | PF01111 | 0.541 |
DOC_CYCLIN_yCln2_LP_2 | 108 | 114 | PF00134 | 0.502 |
DOC_MAPK_DCC_7 | 148 | 158 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 3 | 13 | PF00069 | 0.708 |
DOC_MAPK_MEF2A_6 | 192 | 200 | PF00069 | 0.665 |
DOC_PP1_RVXF_1 | 63 | 69 | PF00149 | 0.599 |
DOC_PP2B_PxIxI_1 | 195 | 201 | PF00149 | 0.535 |
DOC_PP4_FxxP_1 | 283 | 286 | PF00568 | 0.595 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.463 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 148 | 156 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 57 | 66 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 6 | 13 | PF00244 | 0.664 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.521 |
LIG_CSL_BTD_1 | 283 | 286 | PF09270 | 0.457 |
LIG_CSL_BTD_1 | 67 | 70 | PF09270 | 0.419 |
LIG_deltaCOP1_diTrp_1 | 281 | 287 | PF00928 | 0.603 |
LIG_deltaCOP1_diTrp_1 | 315 | 319 | PF00928 | 0.584 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.718 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.629 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.561 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.534 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.808 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.834 |
LIG_Integrin_RGD_1 | 225 | 227 | PF01839 | 0.800 |
LIG_LIR_Apic_2 | 281 | 286 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 262 | 271 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.430 |
LIG_NRBOX | 129 | 135 | PF00104 | 0.465 |
LIG_Pex14_2 | 283 | 287 | PF04695 | 0.590 |
LIG_PTB_Apo_2 | 118 | 125 | PF02174 | 0.488 |
LIG_SH2_NCK_1 | 279 | 283 | PF00017 | 0.648 |
LIG_SH2_NCK_1 | 309 | 313 | PF00017 | 0.425 |
LIG_SH2_SRC | 241 | 244 | PF00017 | 0.664 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.649 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.578 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.486 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.764 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.544 |
MOD_CDK_SPK_2 | 179 | 184 | PF00069 | 0.363 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.545 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.766 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.350 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.504 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.673 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.728 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.765 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.680 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.648 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.712 |
MOD_DYRK1A_RPxSP_1 | 179 | 183 | PF00069 | 0.436 |
MOD_DYRK1A_RPxSP_1 | 192 | 196 | PF00069 | 0.621 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.531 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.687 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.492 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.565 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.512 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.461 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.645 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.580 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.729 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.504 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.576 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.583 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.586 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.422 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.763 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.517 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.608 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.294 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.603 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.658 |
MOD_Plk_2-3 | 203 | 209 | PF00069 | 0.477 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.601 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.462 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.721 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.558 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.549 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.592 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.543 |
TRG_DiLeu_BaEn_2 | 126 | 132 | PF01217 | 0.622 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P910 | Leptomonas seymouri | 37% | 94% |
A0A3S7X3F3 | Leishmania donovani | 84% | 100% |
A4I5M5 | Leishmania infantum | 84% | 100% |
Q4Q796 | Leishmania major | 82% | 100% |