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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B5R9
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:0010941 | regulation of cell death | 4 | 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:0042981 | regulation of apoptotic process | 6 | 1 |
GO:0043067 | regulation of programmed cell death | 5 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051090 | regulation of DNA-binding transcription factor activity | 3 | 1 |
GO:0051091 | positive regulation of DNA-binding transcription factor activity | 4 | 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:0065009 | regulation of molecular function | 2 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 58 | 60 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.670 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.716 |
DEG_SPOP_SBC_1 | 260 | 264 | PF00917 | 0.281 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.803 |
DOC_AGCK_PIF_2 | 70 | 75 | PF00069 | 0.672 |
DOC_MAPK_gen_1 | 138 | 147 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 363 | 372 | PF00069 | 0.585 |
DOC_MAPK_gen_1 | 58 | 67 | PF00069 | 0.677 |
DOC_MAPK_gen_1 | 78 | 88 | PF00069 | 0.639 |
DOC_MAPK_gen_1 | 99 | 107 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 138 | 147 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 82 | 90 | PF00069 | 0.606 |
DOC_PP1_RVXF_1 | 366 | 373 | PF00149 | 0.644 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.532 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.802 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.636 |
DOC_USP7_UBL2_3 | 117 | 121 | PF12436 | 0.529 |
DOC_USP7_UBL2_3 | 337 | 341 | PF12436 | 0.761 |
DOC_USP7_UBL2_3 | 58 | 62 | PF12436 | 0.658 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.261 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 387 | 396 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 414 | 424 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 82 | 87 | PF00244 | 0.522 |
LIG_14-3-3_CterR_2 | 423 | 427 | PF00244 | 0.723 |
LIG_AP2alpha_2 | 68 | 70 | PF02296 | 0.652 |
LIG_BIR_III_4 | 352 | 356 | PF00653 | 0.476 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.507 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.376 |
LIG_deltaCOP1_diTrp_1 | 391 | 398 | PF00928 | 0.719 |
LIG_EVH1_2 | 313 | 317 | PF00568 | 0.704 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.382 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.385 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.658 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.461 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.541 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.461 |
LIG_LIR_Apic_2 | 297 | 301 | PF02991 | 0.620 |
LIG_LIR_Apic_2 | 323 | 327 | PF02991 | 0.720 |
LIG_LIR_Gen_1 | 118 | 123 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 219 | 230 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 118 | 122 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 213 | 218 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 68 | 73 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.430 |
LIG_MLH1_MIPbox_1 | 150 | 154 | PF16413 | 0.507 |
LIG_Pex14_2 | 149 | 153 | PF04695 | 0.482 |
LIG_REV1ctd_RIR_1 | 151 | 158 | PF16727 | 0.530 |
LIG_RPA_C_Fungi | 165 | 177 | PF08784 | 0.557 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.621 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.449 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.629 |
LIG_SH2_GRB2like | 5 | 8 | PF00017 | 0.667 |
LIG_SH2_NCK_1 | 218 | 222 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 5 | 9 | PF00017 | 0.664 |
LIG_SH2_SRC | 73 | 76 | PF00017 | 0.614 |
LIG_SH2_STAT3 | 35 | 38 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.667 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.552 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.644 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 228 | 234 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 176 | 182 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 301 | 307 | PF11976 | 0.692 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.530 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.734 |
LIG_TRAF2_1 | 407 | 410 | PF00917 | 0.674 |
LIG_UBA3_1 | 177 | 185 | PF00899 | 0.448 |
LIG_UBA3_1 | 302 | 310 | PF00899 | 0.726 |
LIG_UBA3_1 | 52 | 58 | PF00899 | 0.626 |
LIG_WRC_WIRS_1 | 116 | 121 | PF05994 | 0.560 |
LIG_WW_1 | 313 | 316 | PF00397 | 0.705 |
MOD_CDK_SPxxK_3 | 131 | 138 | PF00069 | 0.700 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.606 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.636 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.276 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.449 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.779 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.743 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.598 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.785 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.502 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.609 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.491 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.682 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.671 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.722 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.573 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.577 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.689 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.464 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.577 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.413 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.585 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.733 |
MOD_LATS_1 | 80 | 86 | PF00433 | 0.627 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.366 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.694 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.672 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.581 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.503 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.605 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.639 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.305 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.365 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.463 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.509 |
MOD_NEK2_2 | 239 | 244 | PF00069 | 0.437 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.598 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.680 |
MOD_PK_1 | 141 | 147 | PF00069 | 0.564 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.680 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.705 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.773 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.616 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.560 |
MOD_PKB_1 | 385 | 393 | PF00069 | 0.711 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.564 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.363 |
MOD_Plk_1 | 296 | 302 | PF00069 | 0.589 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.585 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.615 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.565 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.350 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.344 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.657 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.709 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.393 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.261 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.328 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.722 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.681 |
MOD_SUMO_rev_2 | 126 | 131 | PF00179 | 0.690 |
MOD_SUMO_rev_2 | 328 | 334 | PF00179 | 0.734 |
MOD_SUMO_rev_2 | 351 | 359 | PF00179 | 0.725 |
MOD_SUMO_rev_2 | 409 | 415 | PF00179 | 0.690 |
TRG_DiLeu_BaEn_1 | 231 | 236 | PF01217 | 0.364 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3M0 | Leptomonas seymouri | 76% | 95% |
A0A0S4JN35 | Bodo saltans | 42% | 100% |
A0A1X0NIX5 | Trypanosomatidae | 38% | 100% |
A0A3S5H7Y3 | Leishmania donovani | 96% | 100% |
A0A422NN82 | Trypanosoma rangeli | 36% | 100% |
A4HM70 | Leishmania braziliensis | 91% | 100% |
A4IAT2 | Leishmania infantum | 96% | 100% |
D0A2C7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AEK8 | Leishmania major | 97% | 100% |
V5BNA7 | Trypanosoma cruzi | 36% | 100% |