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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005882 | intermediate filament | 6 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HP44
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 334 | 338 | PF00656 | 0.443 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.545 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 163 | 165 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 129 | 135 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.321 |
DEG_APCC_DBOX_1 | 297 | 305 | PF00400 | 0.509 |
DEG_SPOP_SBC_1 | 51 | 55 | PF00917 | 0.405 |
DOC_MAPK_gen_1 | 153 | 161 | PF00069 | 0.499 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.650 |
DOC_USP7_UBL2_3 | 133 | 137 | PF12436 | 0.319 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.604 |
LIG_14-3-3_CanoR_1 | 203 | 211 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 350 | 358 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.567 |
LIG_Actin_WH2_2 | 189 | 205 | PF00022 | 0.370 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.494 |
LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.469 |
LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.402 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.459 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.645 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.389 |
LIG_LIR_Nem_3 | 357 | 361 | PF02991 | 0.394 |
LIG_NRBOX | 350 | 356 | PF00104 | 0.396 |
LIG_PCNA_PIPBox_1 | 91 | 100 | PF02747 | 0.404 |
LIG_SH2_GRB2like | 333 | 336 | PF00017 | 0.417 |
LIG_SH2_GRB2like | 97 | 100 | PF00017 | 0.394 |
LIG_SH2_NCK_1 | 333 | 337 | PF00017 | 0.545 |
LIG_SH2_SRC | 333 | 336 | PF00017 | 0.395 |
LIG_SH2_SRC | 97 | 100 | PF00017 | 0.394 |
LIG_SH2_STAT3 | 229 | 232 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.362 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.497 |
MOD_CDK_SPxxK_3 | 52 | 59 | PF00069 | 0.414 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.542 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.659 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.593 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.524 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.589 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.548 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.462 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.494 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.394 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.592 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.725 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.657 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.647 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.643 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.569 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.668 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.463 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.502 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.652 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.537 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.368 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.304 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.559 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.538 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.512 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.467 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.411 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.564 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.459 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.286 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.460 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.401 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.318 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.387 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.609 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.412 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.607 |
MOD_SUMO_rev_2 | 88 | 96 | PF00179 | 0.479 |
TRG_DiLeu_BaEn_3 | 316 | 322 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 126 | 131 | PF01217 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 32 | 37 | PF01217 | 0.470 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.537 |
TRG_NLS_MonoExtC_3 | 161 | 166 | PF00514 | 0.465 |
TRG_NLS_MonoExtN_4 | 162 | 167 | PF00514 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEW3 | Leptomonas seymouri | 45% | 91% |
A0A0S4IWZ6 | Bodo saltans | 23% | 100% |
A0A1X0P838 | Trypanosomatidae | 25% | 93% |
A0A3S5H822 | Leishmania donovani | 67% | 96% |
A0A422NLC8 | Trypanosoma rangeli | 25% | 100% |
A4IDF1 | Leishmania infantum | 69% | 100% |
E9ASV2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 96% |
Q4Q1P4 | Leishmania major | 67% | 100% |
V5B4D1 | Trypanosoma cruzi | 24% | 100% |