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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: E9B0A7
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005524 | ATP binding | 5 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 1 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.710 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 321 | 323 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.705 |
CLV_PCSK_PC7_1 | 143 | 149 | PF00082 | 0.580 |
CLV_PCSK_PC7_1 | 4 | 10 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.442 |
CLV_Separin_Metazoa | 246 | 250 | PF03568 | 0.538 |
DEG_APCC_DBOX_1 | 116 | 124 | PF00400 | 0.621 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.696 |
DEG_SCF_FBW7_1 | 274 | 281 | PF00400 | 0.418 |
DOC_ANK_TNKS_1 | 248 | 255 | PF00023 | 0.528 |
DOC_CDC14_PxL_1 | 198 | 206 | PF14671 | 0.538 |
DOC_CDC14_PxL_1 | 432 | 440 | PF14671 | 0.521 |
DOC_CKS1_1 | 130 | 135 | PF01111 | 0.600 |
DOC_CYCLIN_RxL_1 | 114 | 125 | PF00134 | 0.655 |
DOC_CYCLIN_RxL_1 | 157 | 169 | PF00134 | 0.551 |
DOC_CYCLIN_yCln2_LP_2 | 189 | 195 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 290 | 296 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 311 | 317 | PF00134 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 362 | 368 | PF00134 | 0.705 |
DOC_MAPK_gen_1 | 147 | 153 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 305 | 315 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 305 | 313 | PF00069 | 0.505 |
DOC_PP1_RVXF_1 | 208 | 215 | PF00149 | 0.403 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 290 | 293 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 311 | 314 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 98 | 101 | PF00568 | 0.579 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.725 |
DOC_USP7_UBL2_3 | 458 | 462 | PF12436 | 0.724 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.724 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 40 | 48 | PF00244 | 0.637 |
LIG_Actin_WH2_2 | 306 | 323 | PF00022 | 0.529 |
LIG_APCC_ABBA_1 | 164 | 169 | PF00400 | 0.503 |
LIG_BIR_III_4 | 353 | 357 | PF00653 | 0.683 |
LIG_CSL_BTD_1 | 311 | 314 | PF09270 | 0.517 |
LIG_DLG_GKlike_1 | 47 | 54 | PF00625 | 0.551 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.557 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.552 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.749 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.454 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.437 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.717 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.462 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.767 |
LIG_LIR_Apic_2 | 269 | 274 | PF02991 | 0.606 |
LIG_LIR_Apic_2 | 402 | 407 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 295 | 303 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 46 | 54 | PF02991 | 0.589 |
LIG_LIR_LC3C_4 | 263 | 267 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 310 | 315 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.572 |
LIG_LYPXL_S_1 | 405 | 409 | PF13949 | 0.549 |
LIG_LYPXL_yS_3 | 406 | 409 | PF13949 | 0.521 |
LIG_NRBOX | 222 | 228 | PF00104 | 0.536 |
LIG_Rb_LxCxE_1 | 295 | 310 | PF01857 | 0.242 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.431 |
LIG_SH2_PTP2 | 404 | 407 | PF00017 | 0.269 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.397 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.536 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.611 |
LIG_SH3_CIN85_PxpxPR_1 | 76 | 81 | PF14604 | 0.646 |
LIG_SUMO_SIM_anti_2 | 127 | 132 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 162 | 169 | PF11976 | 0.578 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.734 |
LIG_SUMO_SIM_par_1 | 413 | 419 | PF11976 | 0.557 |
LIG_TYR_ITIM | 330 | 335 | PF00017 | 0.441 |
LIG_WRC_WIRS_1 | 150 | 155 | PF05994 | 0.444 |
LIG_WRC_WIRS_1 | 48 | 53 | PF05994 | 0.577 |
LIG_WW_2 | 360 | 363 | PF00397 | 0.476 |
MOD_CDK_SPK_2 | 76 | 81 | PF00069 | 0.646 |
MOD_CDK_SPxxK_3 | 375 | 382 | PF00069 | 0.707 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.488 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.502 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.682 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.764 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.717 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.603 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.765 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.607 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.746 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.763 |
MOD_Cter_Amidation | 38 | 41 | PF01082 | 0.640 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.589 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.269 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.603 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.636 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.683 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.579 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.536 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.733 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.745 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.549 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.606 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.424 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.647 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.681 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.660 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.692 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.586 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.521 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.549 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.407 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.624 |
MOD_OFUCOSY | 344 | 349 | PF10250 | 0.554 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.516 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.557 |
MOD_PKA_1 | 40 | 46 | PF00069 | 0.665 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.585 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.538 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.742 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.665 |
MOD_Plk_1 | 126 | 132 | PF00069 | 0.399 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.518 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.407 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.522 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.346 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.486 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.460 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.582 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.684 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.660 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.675 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.591 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.728 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.723 |
MOD_SUMO_for_1 | 174 | 177 | PF00179 | 0.663 |
MOD_SUMO_rev_2 | 70 | 76 | PF00179 | 0.561 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.413 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.562 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.662 |
TRG_NES_CRM1_1 | 433 | 445 | PF08389 | 0.517 |
TRG_NLS_MonoExtN_4 | 456 | 461 | PF00514 | 0.775 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4Z3 | Leptomonas seymouri | 45% | 98% |
A0A0S4IUX7 | Bodo saltans | 25% | 100% |
A0A1X0NQH2 | Trypanosomatidae | 28% | 100% |
A0A3S7X213 | Leishmania donovani | 92% | 100% |
A0A422N0P3 | Trypanosoma rangeli | 27% | 100% |
A4HGY8 | Leishmania braziliensis | 78% | 100% |
A4I420 | Leishmania infantum | 93% | 100% |
D0A8Y9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
Q4Q7X7 | Leishmania major | 92% | 100% |
V5ATM8 | Trypanosoma cruzi | 29% | 100% |