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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q8K0
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 6 |
GO:0016043 | cellular component organization | 3 | 6 |
GO:0022607 | cellular component assembly | 4 | 6 |
GO:0043933 | protein-containing complex organization | 4 | 6 |
GO:0051259 | protein complex oligomerization | 6 | 6 |
GO:0051260 | protein homooligomerization | 7 | 6 |
GO:0065003 | protein-containing complex assembly | 5 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.682 |
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.551 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.421 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.677 |
CLV_Separin_Metazoa | 218 | 222 | PF03568 | 0.483 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.722 |
DEG_SPOP_SBC_1 | 290 | 294 | PF00917 | 0.661 |
DOC_CKS1_1 | 351 | 356 | PF01111 | 0.714 |
DOC_CYCLIN_RxL_1 | 297 | 307 | PF00134 | 0.662 |
DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.613 |
DOC_MAPK_DCC_7 | 436 | 446 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 181 | 190 | PF00069 | 0.385 |
DOC_MAPK_HePTP_8 | 233 | 245 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 184 | 192 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 236 | 245 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 242 | 248 | PF00149 | 0.410 |
DOC_PP1_SILK_1 | 456 | 461 | PF00149 | 0.448 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.500 |
DOC_PP2B_LxvP_1 | 254 | 257 | PF13499 | 0.640 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.552 |
DOC_PP2B_LxvP_1 | 360 | 363 | PF13499 | 0.628 |
DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.484 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.610 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.328 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 221 | 229 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 57 | 61 | PF00244 | 0.272 |
LIG_Actin_WH2_2 | 41 | 59 | PF00022 | 0.272 |
LIG_BIR_III_4 | 467 | 471 | PF00653 | 0.689 |
LIG_BRCT_BRCA1_1 | 324 | 328 | PF00533 | 0.752 |
LIG_EVH1_2 | 442 | 446 | PF00568 | 0.424 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.465 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.455 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.430 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.547 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.708 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.560 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.634 |
LIG_LIR_Apic_2 | 246 | 250 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 72 | 82 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 93 | 102 | PF02991 | 0.437 |
LIG_LIR_LC3C_4 | 112 | 116 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.437 |
LIG_MYND_1 | 268 | 272 | PF01753 | 0.615 |
LIG_REV1ctd_RIR_1 | 423 | 431 | PF16727 | 0.433 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 235 | 238 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.398 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.514 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.613 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.590 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.741 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.612 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.591 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.455 |
LIG_SUMO_SIM_anti_2 | 112 | 120 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 41 | 47 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 454 | 463 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 112 | 120 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 302 | 307 | PF11976 | 0.705 |
LIG_SUMO_SIM_par_1 | 406 | 411 | PF11976 | 0.603 |
LIG_WRC_WIRS_1 | 422 | 427 | PF05994 | 0.406 |
MOD_CDK_SPxxK_3 | 35 | 42 | PF00069 | 0.639 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.643 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.612 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.727 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.651 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.441 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.328 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.420 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.638 |
MOD_Cter_Amidation | 5 | 8 | PF01082 | 0.760 |
MOD_GlcNHglycan | 11 | 15 | PF01048 | 0.752 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.567 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.624 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.693 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.604 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.807 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.767 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.706 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.432 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.518 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.440 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.688 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.674 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.616 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.602 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.673 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.742 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.742 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.534 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.328 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.328 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.761 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.385 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.716 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.505 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.719 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.759 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.409 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.465 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.328 |
MOD_NEK2_2 | 421 | 426 | PF00069 | 0.406 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.420 |
MOD_PK_1 | 460 | 466 | PF00069 | 0.480 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.676 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.272 |
MOD_PKB_1 | 8 | 16 | PF00069 | 0.749 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.414 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.678 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.605 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.507 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.381 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.705 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.407 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.441 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.328 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.513 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.698 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.673 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.799 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.649 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.658 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.716 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.328 |
MOD_SUMO_for_1 | 129 | 132 | PF00179 | 0.431 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.716 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 341 | 345 | PF00026 | 0.735 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P854 | Leptomonas seymouri | 59% | 96% |
A0A3S7X191 | Leishmania donovani | 98% | 100% |
A4I3E4 | Leishmania infantum | 98% | 100% |
E9AZN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |