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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AH32
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006351 | DNA-templated transcription | 7 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009058 | biosynthetic process | 2 | 9 |
GO:0009059 | macromolecule biosynthetic process | 4 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0018130 | heterocycle biosynthetic process | 4 | 9 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 9 |
GO:0032774 | RNA biosynthetic process | 5 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044249 | cellular biosynthetic process | 3 | 9 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:0097659 | nucleic acid-templated transcription | 6 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 9 |
GO:1901576 | organic substance biosynthetic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003746 | translation elongation factor activity | 4 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0008135 | translation factor activity, RNA binding | 3 | 9 |
GO:0008270 | zinc ion binding | 6 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0045182 | translation regulator activity | 1 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0046914 | transition metal ion binding | 5 | 9 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.317 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 169 | 171 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.321 |
DEG_SCF_FBW7_1 | 128 | 135 | PF00400 | 0.657 |
DOC_CKS1_1 | 145 | 150 | PF01111 | 0.607 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.653 |
DOC_MAPK_MEF2A_6 | 196 | 204 | PF00069 | 0.489 |
DOC_PP2B_LxvP_1 | 16 | 19 | PF13499 | 0.525 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.620 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.658 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.670 |
DOC_USP7_UBL2_3 | 126 | 130 | PF12436 | 0.667 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 170 | 174 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 189 | 198 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.512 |
LIG_APCC_ABBAyCdc20_2 | 92 | 98 | PF00400 | 0.530 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.662 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.396 |
LIG_Clathr_ClatBox_1 | 248 | 252 | PF01394 | 0.520 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.670 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.659 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.381 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.654 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.587 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.506 |
LIG_LIR_Apic_2 | 61 | 66 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 217 | 226 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.280 |
LIG_MYND_1 | 14 | 18 | PF01753 | 0.527 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.633 |
LIG_SH2_GRB2like | 120 | 123 | PF00017 | 0.629 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.583 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.578 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.559 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.492 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.475 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.614 |
LIG_SUMO_SIM_par_1 | 317 | 322 | PF11976 | 0.371 |
LIG_UBA3_1 | 222 | 230 | PF00899 | 0.437 |
LIG_WW_2 | 19 | 22 | PF00397 | 0.502 |
MOD_CDC14_SPxK_1 | 49 | 52 | PF00782 | 0.619 |
MOD_CDK_SPK_2 | 100 | 105 | PF00069 | 0.694 |
MOD_CDK_SPK_2 | 112 | 117 | PF00069 | 0.472 |
MOD_CDK_SPxK_1 | 46 | 52 | PF00069 | 0.671 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.625 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.567 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.564 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.654 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.506 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.579 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.346 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.737 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.642 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.345 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.236 |
MOD_DYRK1A_RPxSP_1 | 112 | 116 | PF00069 | 0.578 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.602 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.719 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.278 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.740 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.639 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.573 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.592 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.503 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.636 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.495 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.344 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.734 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.579 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.714 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.570 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.572 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.524 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.693 |
MOD_N-GLC_2 | 324 | 326 | PF02516 | 0.278 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.749 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.626 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.545 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.627 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.371 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.661 |
MOD_PKA_1 | 169 | 175 | PF00069 | 0.466 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.467 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.364 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.500 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.411 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.402 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.587 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.466 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.225 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.619 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.508 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.401 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.334 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.644 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.480 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.566 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.702 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.484 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.754 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.482 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.745 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.467 |
MOD_SUMO_rev_2 | 260 | 269 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_1 | 240 | 245 | PF01217 | 0.504 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.629 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.585 |
TRG_NES_CRM1_1 | 246 | 260 | PF08389 | 0.526 |
TRG_NLS_MonoCore_2 | 51 | 56 | PF00514 | 0.596 |
TRG_NLS_MonoExtN_4 | 50 | 56 | PF00514 | 0.640 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFJ1 | Leptomonas seymouri | 59% | 96% |
A0A3Q8IER0 | Leishmania donovani | 99% | 100% |
A0A422P430 | Trypanosoma rangeli | 41% | 100% |
A4HD78 | Leishmania braziliensis | 74% | 99% |
E9AWL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QAW0 | Leishmania major | 93% | 100% |
Q54YG9 | Dictyostelium discoideum | 26% | 100% |
V5DSP1 | Trypanosoma cruzi | 45% | 100% |