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: E9AES7
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0003723 | RNA binding | 4 | 6 |
GO:0003729 | mRNA binding | 5 | 6 |
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.808 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.736 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.736 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.690 |
DEG_APCC_DBOX_1 | 363 | 371 | PF00400 | 0.684 |
DEG_COP1_1 | 404 | 411 | PF00400 | 0.548 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.606 |
DEG_SCF_FBW7_1 | 1 | 7 | PF00400 | 0.667 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.733 |
DEG_SPOP_SBC_1 | 341 | 345 | PF00917 | 0.760 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.676 |
DOC_PP4_FxxP_1 | 368 | 371 | PF00568 | 0.633 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.688 |
DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.690 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.843 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 219 | 226 | PF00244 | 0.653 |
LIG_BRCT_BRCA1_1 | 364 | 368 | PF00533 | 0.688 |
LIG_DLG_GKlike_1 | 25 | 33 | PF00625 | 0.721 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.705 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.704 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.710 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.736 |
LIG_LIR_Apic_2 | 365 | 371 | PF02991 | 0.683 |
LIG_LIR_Gen_1 | 297 | 303 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 31 | 40 | PF02991 | 0.703 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.665 |
LIG_LIR_Gen_1 | 395 | 401 | PF02991 | 0.756 |
LIG_LIR_Gen_1 | 71 | 81 | PF02991 | 0.725 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.703 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.769 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.753 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.594 |
LIG_LYPXL_yS_3 | 65 | 68 | PF13949 | 0.780 |
LIG_SH2_GRB2like | 396 | 399 | PF00017 | 0.602 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.528 |
LIG_SH2_STAT3 | 167 | 170 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.659 |
LIG_SH3_1 | 84 | 90 | PF00018 | 0.601 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.789 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.772 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.731 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.682 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.697 |
LIG_SUMO_SIM_par_1 | 322 | 328 | PF11976 | 0.775 |
LIG_TRAF2_1 | 78 | 81 | PF00917 | 0.732 |
LIG_WRC_WIRS_1 | 295 | 300 | PF05994 | 0.566 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.702 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.779 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.517 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.723 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.756 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.709 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.679 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.707 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.724 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.683 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.587 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.787 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.734 |
MOD_GlcNHglycan | 104 | 108 | PF01048 | 0.627 |
MOD_GlcNHglycan | 144 | 148 | PF01048 | 0.315 |
MOD_GlcNHglycan | 211 | 215 | PF01048 | 0.621 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.653 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.719 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.590 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.764 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.607 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.713 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.709 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.739 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.678 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.555 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.768 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.775 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.508 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.657 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.709 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.723 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.685 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.669 |
MOD_N-GLC_1 | 401 | 406 | PF02516 | 0.578 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.695 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.411 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.643 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.641 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.690 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.729 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.665 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.752 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.702 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.724 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.724 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.786 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.737 |
MOD_Plk_2-3 | 392 | 398 | PF00069 | 0.527 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.760 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.534 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.560 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.690 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.802 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.844 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.702 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.694 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.760 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.783 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.761 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.780 |
TRG_NLS_MonoExtN_4 | 136 | 142 | PF00514 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P318 | Leptomonas seymouri | 41% | 74% |
A0A3S7X8W6 | Leishmania donovani | 90% | 100% |
A4HMD2 | Leishmania braziliensis | 55% | 99% |
A4IAZ9 | Leishmania infantum | 89% | 99% |
E9B5Y2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |