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: A4H688
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 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0008092 | cytoskeletal protein binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 250 | 254 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.413 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.586 |
DEG_SPOP_SBC_1 | 120 | 124 | PF00917 | 0.619 |
DOC_MAPK_gen_1 | 382 | 390 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 324 | 331 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 382 | 390 | PF00069 | 0.496 |
DOC_PP1_RVXF_1 | 374 | 381 | PF00149 | 0.485 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.571 |
DOC_PP2B_LxvP_1 | 234 | 237 | PF13499 | 0.663 |
DOC_PP2B_PxIxI_1 | 338 | 344 | PF00149 | 0.433 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.738 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.378 |
DOC_USP7_MATH_2 | 365 | 371 | PF00917 | 0.383 |
DOC_USP7_MATH_2 | 63 | 69 | PF00917 | 0.600 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 223 | 233 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 404 | 414 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.720 |
LIG_Actin_WH2_2 | 371 | 387 | PF00022 | 0.488 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.484 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.640 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.424 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.485 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.433 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.583 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.566 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.449 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.533 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.576 |
LIG_GBD_Chelix_1 | 147 | 155 | PF00786 | 0.399 |
LIG_HCF-1_HBM_1 | 352 | 355 | PF13415 | 0.632 |
LIG_LIR_Apic_2 | 129 | 135 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 163 | 167 | PF02991 | 0.719 |
LIG_LIR_Gen_1 | 142 | 151 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.675 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.721 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.714 |
LIG_LYPXL_yS_3 | 125 | 128 | PF13949 | 0.717 |
LIG_LYPXL_yS_3 | 13 | 16 | PF13949 | 0.486 |
LIG_LYPXL_yS_3 | 34 | 37 | PF13949 | 0.569 |
LIG_PAM2_1 | 405 | 417 | PF00658 | 0.361 |
LIG_PCNA_yPIPBox_3 | 211 | 221 | PF02747 | 0.515 |
LIG_Pex14_1 | 357 | 361 | PF04695 | 0.555 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.465 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.733 |
LIG_SH2_GRB2like | 144 | 147 | PF00017 | 0.446 |
LIG_SH2_NCK_1 | 49 | 53 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 410 | 414 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.321 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.590 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.539 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.731 |
LIG_SUMO_SIM_anti_2 | 231 | 237 | PF11976 | 0.647 |
LIG_SUMO_SIM_par_1 | 293 | 298 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 327 | 334 | PF11976 | 0.524 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.571 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.417 |
LIG_TRFH_1 | 361 | 365 | PF08558 | 0.585 |
LIG_TYR_ITIM | 136 | 141 | PF00017 | 0.503 |
LIG_TYR_ITSM | 121 | 128 | PF00017 | 0.724 |
LIG_UBA3_1 | 16 | 21 | PF00899 | 0.471 |
LIG_UBA3_1 | 233 | 241 | PF00899 | 0.450 |
LIG_WRC_WIRS_1 | 41 | 46 | PF05994 | 0.633 |
MOD_CDK_SPxxK_3 | 191 | 198 | PF00069 | 0.673 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.657 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.405 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.599 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.791 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.758 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.563 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.672 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.418 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.677 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.646 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.504 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.713 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.539 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.506 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.574 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.660 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.359 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.579 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.510 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.720 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.712 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.580 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.471 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.634 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.700 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.545 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.371 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.625 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.534 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.592 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.576 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.576 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.621 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.537 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.475 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.591 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.586 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.465 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.642 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.482 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.661 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.626 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.532 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.357 |
MOD_Plk_2-3 | 50 | 56 | PF00069 | 0.716 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.393 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.632 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.347 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.490 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.727 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.672 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.634 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.686 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.603 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.550 |
MOD_SUMO_rev_2 | 50 | 59 | PF00179 | 0.567 |
MOD_SUMO_rev_2 | 90 | 97 | PF00179 | 0.572 |
TRG_DiLeu_BaEn_1 | 231 | 236 | PF01217 | 0.641 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.721 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.715 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P323 | Leptomonas seymouri | 33% | 100% |
A0A3Q8I8S8 | Leishmania donovani | 62% | 100% |
E9AGA0 | Leishmania infantum | 63% | 100% |
E9ANB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
Q4QHB4 | Leishmania major | 64% | 100% |