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: 9 |
NetGPI | no | yes: 0, no: 9 |
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: A0A3S5H822
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.564 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.603 |
CLV_PCSK_PC7_1 | 147 | 153 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.593 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.561 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.500 |
DEG_SPOP_SBC_1 | 65 | 69 | PF00917 | 0.554 |
DOC_CYCLIN_yCln2_LP_2 | 81 | 87 | PF00134 | 0.434 |
DOC_MAPK_gen_1 | 180 | 189 | PF00069 | 0.559 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.700 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.543 |
LIG_14-3-3_CanoR_1 | 14 | 19 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 165 | 175 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 180 | 184 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 368 | 374 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.626 |
LIG_APCC_ABBA_1 | 187 | 192 | PF00400 | 0.487 |
LIG_APCC_ABBAyCdc20_2 | 186 | 192 | PF00400 | 0.490 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.493 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.642 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.616 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.588 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.528 |
LIG_PCNA_PIPBox_1 | 109 | 118 | PF02747 | 0.570 |
LIG_PDZ_Class_3 | 381 | 386 | PF00595 | 0.529 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.372 |
LIG_SH2_GRB2like | 115 | 118 | PF00017 | 0.562 |
LIG_SH2_NCK_1 | 351 | 355 | PF00017 | 0.646 |
LIG_SH2_SRC | 115 | 118 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.415 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.447 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.473 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.472 |
LIG_TRAF2_1 | 216 | 219 | PF00917 | 0.588 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.571 |
LIG_UBA3_1 | 145 | 151 | PF00899 | 0.440 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.503 |
MOD_CDK_SPxxK_3 | 71 | 78 | PF00069 | 0.522 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.349 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.613 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.725 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.516 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.381 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.605 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.573 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.526 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.554 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.503 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.637 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.654 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.515 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.697 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.736 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.670 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.701 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.502 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.695 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.588 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.621 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.445 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.612 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.672 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.581 |
MOD_PKA_1 | 14 | 20 | PF00069 | 0.539 |
MOD_PKA_1 | 151 | 157 | PF00069 | 0.376 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.620 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.579 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.539 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.620 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.545 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.612 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.584 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.532 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.609 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.688 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.515 |
MOD_SUMO_for_1 | 291 | 294 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_1 | 170 | 175 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_3 | 334 | 340 | PF01217 | 0.585 |
TRG_DiLeu_BaLyEn_6 | 144 | 149 | PF01217 | 0.588 |
TRG_DiLeu_LyEn_5 | 170 | 175 | PF01217 | 0.521 |
TRG_ER_diArg_1 | 103 | 105 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEW3 | Leptomonas seymouri | 45% | 95% |
A0A0S4IWZ6 | Bodo saltans | 20% | 100% |
A0A1X0P838 | Trypanosomatidae | 24% | 98% |
A0A422NLC8 | Trypanosoma rangeli | 28% | 100% |
A4HP44 | Leishmania braziliensis | 67% | 100% |
E9ASV2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q1P4 | Leishmania major | 90% | 100% |
V5B4D1 | Trypanosoma cruzi | 27% | 100% |