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: A0A3S7X8W6
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 | 0.661 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.671 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.606 |
DEG_APCC_DBOX_1 | 363 | 371 | PF00400 | 0.577 |
DEG_SCF_FBW7_1 | 1 | 7 | PF00400 | 0.600 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.648 |
DEG_SPOP_SBC_1 | 341 | 345 | PF00917 | 0.626 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.597 |
DOC_PP4_FxxP_1 | 368 | 371 | PF00568 | 0.531 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.602 |
DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.606 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.524 |
LIG_14-3-3_CanoR_1 | 219 | 226 | PF00244 | 0.561 |
LIG_BRCT_BRCA1_1 | 364 | 368 | PF00533 | 0.583 |
LIG_DLG_GKlike_1 | 25 | 33 | PF00625 | 0.611 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.622 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.576 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.735 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.635 |
LIG_LIR_Apic_2 | 365 | 371 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 33 | 40 | PF02991 | 0.732 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 395 | 401 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 71 | 81 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.733 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.633 |
LIG_LYPXL_yS_3 | 65 | 68 | PF13949 | 0.642 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.442 |
LIG_SH2_STAT3 | 167 | 170 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.563 |
LIG_SH3_1 | 251 | 257 | PF00018 | 0.560 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.661 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.670 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.578 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.613 |
LIG_SUMO_SIM_par_1 | 322 | 328 | PF11976 | 0.627 |
LIG_SUMO_SIM_par_1 | 343 | 350 | PF11976 | 0.599 |
LIG_TRAF2_1 | 78 | 81 | PF00917 | 0.623 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.599 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.694 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.487 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.656 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.653 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.494 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.499 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.567 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.637 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.620 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.607 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.671 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.625 |
MOD_GlcNHglycan | 104 | 108 | PF01048 | 0.543 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.579 |
MOD_GlcNHglycan | 144 | 148 | PF01048 | 0.238 |
MOD_GlcNHglycan | 211 | 215 | PF01048 | 0.496 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.564 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.708 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.593 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.714 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.709 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.625 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.612 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.641 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.593 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.454 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.723 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.719 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.615 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.550 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.601 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.620 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.586 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.646 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.562 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.589 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.304 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.650 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.588 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.620 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.616 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.655 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.613 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.613 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.613 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.625 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.686 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.740 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.691 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.599 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.601 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.682 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.583 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.642 |
TRG_NLS_MonoExtN_4 | 136 | 142 | PF00514 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P318 | Leptomonas seymouri | 38% | 74% |
A4HMD2 | Leishmania braziliensis | 56% | 100% |
A4IAZ9 | Leishmania infantum | 99% | 100% |
E9AES7 | Leishmania major | 90% | 100% |
E9B5Y2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |