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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005885 | Arp2/3 protein complex | 2 | 6 |
GO:0032991 | protein-containing complex | 1 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9AGA0
Term | Name | Level | Count |
---|---|---|---|
GO:0007015 | actin filament organization | 5 | 6 |
GO:0008064 | regulation of actin polymerization or depolymerization | 6 | 6 |
GO:0008154 | actin polymerization or depolymerization | 6 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016043 | cellular component organization | 3 | 6 |
GO:0022607 | cellular component assembly | 4 | 6 |
GO:0030041 | actin filament polymerization | 7 | 6 |
GO:0030832 | regulation of actin filament length | 5 | 6 |
GO:0030833 | regulation of actin filament polymerization | 7 | 6 |
GO:0032271 | regulation of protein polymerization | 6 | 6 |
GO:0032535 | regulation of cellular component size | 4 | 6 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 6 |
GO:0032970 | regulation of actin filament-based process | 4 | 6 |
GO:0033043 | regulation of organelle organization | 5 | 6 |
GO:0034314 | Arp2/3 complex-mediated actin nucleation | 7 | 6 |
GO:0043254 | regulation of protein-containing complex assembly | 5 | 6 |
GO:0043933 | protein-containing complex organization | 4 | 6 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 6 |
GO:0045010 | actin nucleation | 6 | 6 |
GO:0050789 | regulation of biological process | 2 | 6 |
GO:0050794 | regulation of cellular process | 3 | 6 |
GO:0051128 | regulation of cellular component organization | 4 | 6 |
GO:0051258 | protein polymerization | 6 | 6 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 6 |
GO:0065003 | protein-containing complex assembly | 5 | 6 |
GO:0065007 | biological regulation | 1 | 6 |
GO:0065008 | regulation of biological quality | 2 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 6 |
GO:0090066 | regulation of anatomical structure size | 3 | 6 |
GO:0097435 | supramolecular fiber organization | 4 | 6 |
GO:0110053 | regulation of actin filament organization | 6 | 6 |
GO:1902903 | regulation of supramolecular fiber organization | 5 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0005515 | protein binding | 2 | 3 |
GO:0008092 | cytoskeletal protein binding | 3 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.612 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 308 | 310 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.376 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.506 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 128 | 136 | PF00134 | 0.596 |
DOC_CYCLIN_yCln2_LP_2 | 172 | 178 | PF00134 | 0.524 |
DOC_MAPK_gen_1 | 308 | 316 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 367 | 375 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 308 | 316 | PF00069 | 0.634 |
DOC_MAPK_MEF2A_6 | 367 | 375 | PF00069 | 0.495 |
DOC_PP1_RVXF_1 | 359 | 366 | PF00149 | 0.493 |
DOC_PP2B_LxvP_1 | 172 | 175 | PF13499 | 0.539 |
DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.636 |
DOC_PP2B_PxIxI_1 | 110 | 116 | PF00149 | 0.605 |
DOC_PP4_FxxP_1 | 117 | 120 | PF00568 | 0.679 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.403 |
DOC_USP7_MATH_2 | 156 | 162 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 103 | 113 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 389 | 399 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 186 | 201 | PF00022 | 0.511 |
LIG_Actin_WH2_2 | 355 | 372 | PF00022 | 0.492 |
LIG_APCC_ABBA_1 | 375 | 380 | PF00400 | 0.490 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.679 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.624 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.458 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.645 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.532 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.438 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.639 |
LIG_HCF-1_HBM_1 | 337 | 340 | PF13415 | 0.613 |
LIG_LIR_Apic_2 | 148 | 152 | PF02991 | 0.687 |
LIG_LIR_Gen_1 | 302 | 312 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 107 | 113 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.537 |
LIG_LYPXL_yS_3 | 110 | 113 | PF13949 | 0.641 |
LIG_NRBOX | 201 | 207 | PF00104 | 0.460 |
LIG_Pex14_1 | 342 | 346 | PF04695 | 0.543 |
LIG_SH2_CRK | 149 | 153 | PF00017 | 0.629 |
LIG_SH2_SRC | 300 | 303 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 395 | 399 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.489 |
LIG_SH3_2 | 19 | 24 | PF14604 | 0.706 |
LIG_SH3_3 | 16 | 22 | PF00018 | 0.713 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 216 | 222 | PF11976 | 0.553 |
LIG_SUMO_SIM_par_1 | 277 | 283 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 312 | 319 | PF11976 | 0.618 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.541 |
LIG_TRFH_1 | 346 | 350 | PF08558 | 0.585 |
LIG_TYR_ITSM | 106 | 113 | PF00017 | 0.676 |
LIG_WRC_WIRS_1 | 25 | 30 | PF05994 | 0.636 |
MOD_CDK_SPxxK_3 | 176 | 183 | PF00069 | 0.641 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.622 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.624 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.618 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.542 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.767 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.486 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.515 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.807 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.640 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.639 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.705 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.619 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.586 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.651 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.526 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.616 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.551 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.716 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.454 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.596 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.492 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.483 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.736 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.712 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.577 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.671 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.507 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.618 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.553 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.544 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.396 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.422 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.746 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.622 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.683 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.552 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.493 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.447 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.535 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.714 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.656 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.539 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.561 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.459 |
MOD_PKB_1 | 103 | 111 | PF00069 | 0.539 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.507 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.683 |
MOD_Plk_2-3 | 34 | 40 | PF00069 | 0.677 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.610 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.669 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.407 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.493 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.506 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.702 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.640 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.591 |
MOD_SUMO_rev_2 | 302 | 310 | PF00179 | 0.561 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 358 | 363 | PF01217 | 0.375 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.654 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.380 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.602 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P323 | Leptomonas seymouri | 32% | 95% |
A0A3Q8I8S8 | Leishmania donovani | 99% | 100% |
A4H688 | Leishmania braziliensis | 63% | 100% |
E9ANB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QHB4 | Leishmania major | 88% | 100% |