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:0005856 | cytoskeleton | 5 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0030864 | cortical actin cytoskeleton | 7 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B127
Term | Name | Level | Count |
---|---|---|---|
GO:0008064 | regulation of actin polymerization or depolymerization | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0030832 | regulation of actin filament length | 5 | 1 |
GO:0030833 | regulation of actin filament polymerization | 7 | 1 |
GO:0032271 | regulation of protein polymerization | 6 | 1 |
GO:0032535 | regulation of cellular component size | 4 | 1 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 1 |
GO:0032970 | regulation of actin filament-based process | 4 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0043254 | regulation of protein-containing complex assembly | 5 | 1 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090066 | regulation of anatomical structure size | 3 | 1 |
GO:0110053 | regulation of actin filament organization | 6 | 1 |
GO:1902903 | regulation of supramolecular fiber organization | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0008092 | cytoskeletal protein binding | 3 | 10 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0051015 | actin filament binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.458 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.691 |
CLV_PCSK_FUR_1 | 145 | 149 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.461 |
DEG_Kelch_Keap1_1 | 237 | 242 | PF01344 | 0.550 |
DEG_SCF_TRCP1_1 | 105 | 110 | PF00400 | 0.602 |
DOC_CYCLIN_yCln2_LP_2 | 355 | 361 | PF00134 | 0.701 |
DOC_MAPK_gen_1 | 167 | 177 | PF00069 | 0.667 |
DOC_MAPK_gen_1 | 350 | 359 | PF00069 | 0.716 |
DOC_MAPK_gen_1 | 41 | 48 | PF00069 | 0.423 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.714 |
DOC_MAPK_MEF2A_6 | 170 | 179 | PF00069 | 0.529 |
DOC_MAPK_RevD_3 | 231 | 247 | PF00069 | 0.579 |
DOC_PP1_RVXF_1 | 233 | 239 | PF00149 | 0.536 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.465 |
DOC_PP2B_LxvP_1 | 355 | 358 | PF13499 | 0.705 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.312 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 147 | 152 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 183 | 189 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 235 | 239 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 306 | 313 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 332 | 336 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 348 | 358 | PF00244 | 0.588 |
LIG_APCC_ABBA_1 | 127 | 132 | PF00400 | 0.571 |
LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.579 |
LIG_BRCT_BRCA1_1 | 322 | 326 | PF00533 | 0.577 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.568 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 226 | 234 | PF00928 | 0.530 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.486 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.733 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.449 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.604 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.629 |
LIG_GBD_Chelix_1 | 401 | 409 | PF00786 | 0.443 |
LIG_LIR_Gen_1 | 88 | 98 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.539 |
LIG_LYPXL_S_1 | 269 | 273 | PF13949 | 0.361 |
LIG_LYPXL_yS_3 | 270 | 273 | PF13949 | 0.561 |
LIG_PDZ_Class_3 | 404 | 409 | PF00595 | 0.448 |
LIG_Pex14_2 | 234 | 238 | PF04695 | 0.561 |
LIG_SH2_PTP2 | 50 | 53 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.436 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.740 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.779 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.743 |
LIG_SUMO_SIM_anti_2 | 201 | 208 | PF11976 | 0.384 |
LIG_SUMO_SIM_anti_2 | 388 | 395 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.694 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.657 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.574 |
LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.589 |
LIG_TRAF2_1 | 386 | 389 | PF00917 | 0.608 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.561 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.695 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.427 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.712 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.590 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.550 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.529 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.563 |
MOD_Cter_Amidation | 145 | 148 | PF01082 | 0.655 |
MOD_DYRK1A_RPxSP_1 | 170 | 174 | PF00069 | 0.770 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.624 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.567 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.639 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.589 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.748 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.559 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.567 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.581 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.726 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.625 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.503 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.536 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.517 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.542 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.552 |
MOD_N-GLC_2 | 74 | 76 | PF02516 | 0.412 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.472 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.438 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.596 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.704 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.588 |
MOD_NEK2_2 | 36 | 41 | PF00069 | 0.518 |
MOD_PKA_1 | 147 | 153 | PF00069 | 0.706 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.672 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.756 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.472 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.379 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.588 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.754 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.440 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.621 |
MOD_PKB_1 | 119 | 127 | PF00069 | 0.341 |
MOD_PKB_1 | 145 | 153 | PF00069 | 0.694 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.541 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.588 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.588 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.501 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.539 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.585 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.579 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.491 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.570 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.742 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.579 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.686 |
MOD_SUMO_for_1 | 166 | 169 | PF00179 | 0.734 |
MOD_SUMO_rev_2 | 19 | 26 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 308 | 313 | PF00179 | 0.418 |
TRG_DiLeu_BaEn_1 | 389 | 394 | PF01217 | 0.435 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.546 |
TRG_NES_CRM1_1 | 92 | 105 | PF08389 | 0.540 |
TRG_NLS_MonoExtC_3 | 143 | 148 | PF00514 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5G8 | Leptomonas seymouri | 66% | 100% |
A0A1X0P342 | Trypanosomatidae | 39% | 100% |
A0A3Q8IFZ1 | Leishmania donovani | 93% | 100% |
A4HII8 | Leishmania braziliensis | 83% | 100% |
A4I5T2 | Leishmania infantum | 94% | 100% |
C9ZR53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 91% |
Q4Q738 | Leishmania major | 92% | 100% |
V5BMX2 | Trypanosoma cruzi | 41% | 100% |