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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QAW0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006351 | DNA-templated transcription | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009058 | biosynthetic process | 2 | 10 |
GO:0009059 | macromolecule biosynthetic process | 4 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0018130 | heterocycle biosynthetic process | 4 | 10 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 10 |
GO:0032774 | RNA biosynthetic process | 5 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044249 | cellular biosynthetic process | 3 | 10 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:0097659 | nucleic acid-templated transcription | 6 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 10 |
GO:1901576 | organic substance biosynthetic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003746 | translation elongation factor activity | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0008135 | translation factor activity, RNA binding | 3 | 10 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0045182 | translation regulator activity | 1 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.373 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.654 |
CLV_PCSK_PC1ET2_1 | 169 | 171 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.391 |
DEG_SCF_FBW7_1 | 128 | 135 | PF00400 | 0.733 |
DOC_ANK_TNKS_1 | 235 | 242 | PF00023 | 0.534 |
DOC_CKS1_1 | 145 | 150 | PF01111 | 0.671 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.785 |
DOC_MAPK_MEF2A_6 | 196 | 204 | PF00069 | 0.516 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.724 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.780 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.798 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.789 |
DOC_USP7_UBL2_3 | 126 | 130 | PF12436 | 0.761 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 112 | 117 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 170 | 174 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 189 | 198 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 73 | 81 | PF00244 | 0.562 |
LIG_Actin_WH2_2 | 57 | 75 | PF00022 | 0.553 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.741 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.473 |
LIG_Clathr_ClatBox_1 | 248 | 252 | PF01394 | 0.561 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.699 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.749 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.444 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.707 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.666 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.591 |
LIG_LIR_Apic_2 | 61 | 66 | PF02991 | 0.777 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.737 |
LIG_LIR_Gen_1 | 217 | 226 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.347 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.732 |
LIG_SH2_GRB2like | 120 | 123 | PF00017 | 0.726 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.660 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.656 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.601 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.557 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.550 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.719 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.717 |
LIG_SUMO_SIM_par_1 | 317 | 322 | PF11976 | 0.444 |
LIG_UBA3_1 | 222 | 230 | PF00899 | 0.490 |
MOD_CDC14_SPxK_1 | 49 | 52 | PF00782 | 0.719 |
MOD_CDK_SPK_2 | 100 | 105 | PF00069 | 0.763 |
MOD_CDK_SPK_2 | 112 | 117 | PF00069 | 0.538 |
MOD_CDK_SPxK_1 | 46 | 52 | PF00069 | 0.757 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.725 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.535 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.659 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.565 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.674 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.620 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.637 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.428 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.797 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.739 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.742 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.401 |
MOD_CK2_1 | 300 | 306 | PF00069 | 0.394 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.293 |
MOD_DYRK1A_RPxSP_1 | 112 | 116 | PF00069 | 0.676 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.681 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.344 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.804 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.646 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.653 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.613 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.584 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.748 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.534 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.394 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.726 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.598 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.571 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.658 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.738 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.650 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.645 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.577 |
MOD_N-GLC_2 | 324 | 326 | PF02516 | 0.325 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.790 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.730 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.563 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.761 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.444 |
MOD_PKA_1 | 169 | 175 | PF00069 | 0.570 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.569 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.653 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.565 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.354 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.383 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.566 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.701 |
MOD_Plk_1 | 288 | 294 | PF00069 | 0.532 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.271 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.721 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.531 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.461 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.361 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.719 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.738 |
MOD_ProDKin_1 | 112 | 118 | PF00069 | 0.549 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.580 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.565 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.803 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.550 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.793 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.475 |
MOD_SUMO_rev_2 | 260 | 269 | PF00179 | 0.591 |
TRG_DiLeu_BaEn_1 | 240 | 245 | PF01217 | 0.561 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.726 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.704 |
TRG_NES_CRM1_1 | 246 | 260 | PF08389 | 0.536 |
TRG_NLS_MonoCore_2 | 51 | 56 | PF00514 | 0.678 |
TRG_NLS_MonoExtN_4 | 50 | 56 | PF00514 | 0.737 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFJ1 | Leptomonas seymouri | 63% | 96% |
A0A1X0NIZ8 | Trypanosomatidae | 46% | 100% |
A0A3Q8IER0 | Leishmania donovani | 93% | 100% |
A0A422P430 | Trypanosoma rangeli | 41% | 100% |
A4HD78 | Leishmania braziliensis | 74% | 100% |
E9AH32 | Leishmania infantum | 93% | 100% |
E9AWL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 99% |
V5DSP1 | Trypanosoma cruzi | 45% | 100% |