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: A4IAZ9
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 | 104 | 108 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.656 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.546 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 141 | 143 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.601 |
DEG_APCC_DBOX_1 | 366 | 374 | PF00400 | 0.565 |
DEG_SCF_FBW7_1 | 1 | 7 | PF00400 | 0.581 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.626 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.612 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.578 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.520 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.599 |
DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.601 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 222 | 229 | PF00244 | 0.550 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.571 |
LIG_DLG_GKlike_1 | 25 | 33 | PF00625 | 0.601 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.604 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.569 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.604 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.622 |
LIG_LIR_Apic_2 | 368 | 374 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 33 | 40 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 339 | 349 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 398 | 404 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 71 | 81 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 164 | 170 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.753 |
LIG_LYPXL_yS_3 | 65 | 68 | PF13949 | 0.632 |
LIG_NRBOX | 356 | 362 | PF00104 | 0.477 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.440 |
LIG_SH2_STAT3 | 170 | 173 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.542 |
LIG_SH3_1 | 254 | 260 | PF00018 | 0.544 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.646 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.655 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.567 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.602 |
LIG_SUMO_SIM_par_1 | 325 | 331 | PF11976 | 0.613 |
LIG_SUMO_SIM_par_1 | 346 | 353 | PF11976 | 0.494 |
LIG_TRAF2_1 | 78 | 81 | PF00917 | 0.725 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.587 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.760 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.478 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.606 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.612 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.477 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.490 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.552 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.607 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.610 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.595 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.652 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.729 |
MOD_GlcNHglycan | 107 | 111 | PF01048 | 0.563 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.572 |
MOD_GlcNHglycan | 147 | 151 | PF01048 | 0.238 |
MOD_GlcNHglycan | 214 | 218 | PF01048 | 0.493 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.554 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.660 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.524 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.702 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.697 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.605 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.606 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.657 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.585 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.448 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.679 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.671 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.542 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.536 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.585 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.615 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.577 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.675 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.542 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.585 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.304 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.608 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.641 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.513 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.606 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.593 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.644 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.601 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.605 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.605 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.620 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.665 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.759 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.663 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.517 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.593 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.771 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 323 | 328 | PF01217 | 0.573 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.774 |
TRG_NLS_MonoExtN_4 | 139 | 145 | PF00514 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P318 | Leptomonas seymouri | 42% | 75% |
A0A3S7X8W6 | Leishmania donovani | 99% | 100% |
A4HMD2 | Leishmania braziliensis | 55% | 99% |
E9AES7 | Leishmania major | 89% | 99% |
E9B5Y2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |