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: 5 |
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 | yes | yes: 8, no: 0 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 9 |
GO:0042995 | cell projection | 2 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 9 |
Related structures:
AlphaFold database: A4HHL3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.242 |
CLV_Separin_Metazoa | 391 | 395 | PF03568 | 0.372 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.457 |
DEG_SPOP_SBC_1 | 213 | 217 | PF00917 | 0.580 |
DOC_CYCLIN_RxL_1 | 388 | 402 | PF00134 | 0.482 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 333 | 342 | PF00134 | 0.253 |
DOC_CYCLIN_yCln2_LP_2 | 151 | 157 | PF00134 | 0.593 |
DOC_CYCLIN_yCln2_LP_2 | 438 | 444 | PF00134 | 0.256 |
DOC_MAPK_MEF2A_6 | 80 | 89 | PF00069 | 0.301 |
DOC_PP1_RVXF_1 | 28 | 35 | PF00149 | 0.409 |
DOC_PP1_RVXF_1 | 392 | 399 | PF00149 | 0.289 |
DOC_USP7_UBL2_3 | 261 | 265 | PF12436 | 0.275 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 111 | 116 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 143 | 151 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 273 | 279 | PF00244 | 0.230 |
LIG_14-3-3_CanoR_1 | 289 | 298 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 68 | 73 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 97 | 104 | PF00244 | 0.512 |
LIG_14-3-3_CterR_2 | 478 | 482 | PF00244 | 0.501 |
LIG_Actin_WH2_2 | 274 | 291 | PF00022 | 0.240 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.559 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.471 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.243 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.539 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.590 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.479 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.412 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.335 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.570 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.570 |
LIG_IRF3_LxIS_1 | 270 | 277 | PF10401 | 0.531 |
LIG_LIR_Apic_2 | 476 | 480 | PF02991 | 0.676 |
LIG_LIR_Gen_1 | 284 | 291 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 395 | 406 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 277 | 281 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 284 | 288 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 420 | 424 | PF02991 | 0.286 |
LIG_SH2_CRK | 477 | 481 | PF00017 | 0.407 |
LIG_SH2_PTP2 | 444 | 447 | PF00017 | 0.260 |
LIG_SH2_PTP2 | 467 | 470 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.409 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.649 |
LIG_SUMO_SIM_par_1 | 152 | 159 | PF11976 | 0.587 |
LIG_SUMO_SIM_par_1 | 224 | 229 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 234 | 240 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 296 | 301 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 310 | 315 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 352 | 357 | PF11976 | 0.330 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.581 |
LIG_TYR_ITIM | 419 | 424 | PF00017 | 0.538 |
LIG_TYR_ITIM | 442 | 447 | PF00017 | 0.263 |
LIG_TYR_ITIM | 465 | 470 | PF00017 | 0.261 |
LIG_UBA3_1 | 1 | 6 | PF00899 | 0.455 |
LIG_UBA3_1 | 341 | 350 | PF00899 | 0.263 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.443 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.499 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.565 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.580 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.583 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.259 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.543 |
MOD_GlcNHglycan | 299 | 303 | PF01048 | 0.409 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.441 |
MOD_GlcNHglycan | 400 | 404 | PF01048 | 0.406 |
MOD_GlcNHglycan | 47 | 51 | PF01048 | 0.460 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.552 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.455 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.555 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.516 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.452 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.532 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.379 |
MOD_LATS_1 | 22 | 28 | PF00433 | 0.439 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.375 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.338 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.475 |
MOD_N-GLC_1 | 336 | 341 | PF02516 | 0.423 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.324 |
MOD_N-GLC_1 | 433 | 438 | PF02516 | 0.483 |
MOD_N-GLC_1 | 450 | 455 | PF02516 | 0.264 |
MOD_N-GLC_2 | 204 | 206 | PF02516 | 0.261 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.455 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.560 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.500 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.450 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.448 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.548 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.268 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.368 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.438 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.494 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.239 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.410 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.366 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.290 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.213 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.308 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.286 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.545 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.440 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.591 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.444 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.498 |
MOD_PK_1 | 111 | 117 | PF00069 | 0.314 |
MOD_PK_1 | 68 | 74 | PF00069 | 0.605 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.579 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.689 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.264 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.505 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.317 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.472 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.475 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.553 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.616 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.620 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.620 |
MOD_SUMO_for_1 | 209 | 212 | PF00179 | 0.633 |
MOD_SUMO_rev_2 | 301 | 311 | PF00179 | 0.324 |
TRG_DiLeu_BaEn_2 | 51 | 57 | PF01217 | 0.338 |
TRG_ENDOCYTIC_2 | 421 | 424 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.531 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.572 |
TRG_NES_CRM1_1 | 240 | 254 | PF08389 | 0.546 |
TRG_NES_CRM1_1 | 391 | 405 | PF08389 | 0.555 |
TRG_NLS_MonoExtN_4 | 139 | 146 | PF00514 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P012 | Trypanosomatidae | 30% | 100% |
A0A3R7KGL7 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H7L7 | Leishmania donovani | 70% | 100% |
A4I4S2 | Leishmania infantum | 69% | 100% |
E9AE75 | Leishmania major | 70% | 100% |
E9ALL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
V5BBX4 | Trypanosoma cruzi | 30% | 100% |