Chaperone/Protein Folding, PA26 p53-induced (sestrin), putative
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0005737 | cytoplasm | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A4HXU1
Term | Name | Level | Count |
---|---|---|---|
GO:0009966 | regulation of signal transduction | 4 | 7 |
GO:0009968 | negative regulation of signal transduction | 5 | 7 |
GO:0010646 | regulation of cell communication | 4 | 7 |
GO:0010648 | negative regulation of cell communication | 5 | 7 |
GO:0023051 | regulation of signaling | 3 | 7 |
GO:0023057 | negative regulation of signaling | 4 | 7 |
GO:0032006 | regulation of TOR signaling | 6 | 7 |
GO:0032007 | negative regulation of TOR signaling | 7 | 7 |
GO:0048519 | negative regulation of biological process | 3 | 7 |
GO:0048523 | negative regulation of cellular process | 4 | 7 |
GO:0048583 | regulation of response to stimulus | 3 | 7 |
GO:0048585 | negative regulation of response to stimulus | 4 | 7 |
GO:0050789 | regulation of biological process | 2 | 7 |
GO:0050794 | regulation of cellular process | 3 | 7 |
GO:0065007 | biological regulation | 1 | 7 |
GO:0080134 | regulation of response to stress | 4 | 7 |
GO:1901031 | regulation of response to reactive oxygen species | 6 | 7 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 7 |
GO:1902532 | negative regulation of intracellular signal transduction | 6 | 7 |
GO:1902882 | regulation of response to oxidative stress | 5 | 7 |
GO:0001101 | response to acid chemical | 3 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0007154 | cell communication | 2 | 1 |
GO:0009267 | cellular response to starvation | 4 | 1 |
GO:0009605 | response to external stimulus | 2 | 1 |
GO:0009719 | response to endogenous stimulus | 2 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009896 | positive regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0009991 | response to extracellular stimulus | 3 | 1 |
GO:0010033 | response to organic substance | 3 | 1 |
GO:0010243 | response to organonitrogen compound | 4 | 1 |
GO:0010506 | regulation of autophagy | 6 | 1 |
GO:0010508 | positive regulation of autophagy | 7 | 1 |
GO:0016239 | positive regulation of macroautophagy | 8 | 1 |
GO:0016241 | regulation of macroautophagy | 7 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031331 | positive regulation of cellular catabolic process | 6 | 1 |
GO:0031667 | response to nutrient levels | 4 | 1 |
GO:0031668 | cellular response to extracellular stimulus | 3 | 1 |
GO:0031669 | cellular response to nutrient levels | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034198 | cellular response to amino acid starvation | 5 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0042594 | response to starvation | 3 | 1 |
GO:0043200 | response to amino acid | 4 | 1 |
GO:0043201 | response to leucine | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0070887 | cellular response to chemical stimulus | 3 | 1 |
GO:0071229 | cellular response to acid chemical | 4 | 1 |
GO:0071230 | cellular response to amino acid stimulus | 5 | 1 |
GO:0071233 | cellular response to leucine | 6 | 1 |
GO:0071310 | cellular response to organic substance | 4 | 1 |
GO:0071417 | cellular response to organonitrogen compound | 4 | 1 |
GO:0071495 | cellular response to endogenous stimulus | 3 | 1 |
GO:0071496 | cellular response to external stimulus | 3 | 1 |
GO:1901698 | response to nitrogen compound | 3 | 1 |
GO:1901699 | cellular response to nitrogen compound | 4 | 1 |
GO:1901700 | response to oxygen-containing compound | 3 | 1 |
GO:1901701 | cellular response to oxygen-containing compound | 4 | 1 |
GO:1903432 | regulation of TORC1 signaling | 7 | 1 |
GO:1904262 | negative regulation of TORC1 signaling | 8 | 1 |
GO:1990253 | cellular response to leucine starvation | 6 | 1 |
GO:1990928 | response to amino acid starvation | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016597 | amino acid binding | 4 | 1 |
GO:0016684 | oxidoreductase activity, acting on peroxide as acceptor | 3 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043177 | organic acid binding | 3 | 1 |
GO:0070728 | leucine binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.490 |
CLV_C14_Caspase3-7 | 1223 | 1227 | PF00656 | 0.686 |
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.539 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 656 | 660 | PF00656 | 0.617 |
CLV_C14_Caspase3-7 | 858 | 862 | PF00656 | 0.570 |
CLV_MEL_PAP_1 | 796 | 802 | PF00089 | 0.546 |
CLV_NRD_NRD_1 | 1052 | 1054 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 1165 | 1167 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 1288 | 1290 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.712 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 859 | 861 | PF00675 | 0.668 |
CLV_PCSK_FUR_1 | 630 | 634 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 1052 | 1054 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 1165 | 1167 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 1216 | 1218 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 630 | 632 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 859 | 861 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 1216 | 1218 | PF00082 | 0.450 |
CLV_PCSK_PC1ET2_1 | 706 | 708 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 1116 | 1120 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 1166 | 1170 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 1276 | 1280 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 646 | 650 | PF00082 | 0.779 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 903 | 907 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 936 | 940 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 991 | 995 | PF00082 | 0.588 |
CLV_Separin_Metazoa | 1186 | 1190 | PF03568 | 0.677 |
DEG_APCC_DBOX_1 | 708 | 716 | PF00400 | 0.405 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.559 |
DEG_SCF_TRCP1_1 | 305 | 310 | PF00400 | 0.494 |
DEG_SPOP_SBC_1 | 221 | 225 | PF00917 | 0.518 |
DEG_SPOP_SBC_1 | 509 | 513 | PF00917 | 0.601 |
DOC_ANK_TNKS_1 | 107 | 114 | PF00023 | 0.498 |
DOC_CDC14_PxL_1 | 467 | 475 | PF14671 | 0.519 |
DOC_CKS1_1 | 1193 | 1198 | PF01111 | 0.733 |
DOC_CKS1_1 | 1250 | 1255 | PF01111 | 0.693 |
DOC_CYCLIN_RxL_1 | 115 | 124 | PF00134 | 0.560 |
DOC_CYCLIN_RxL_1 | 746 | 756 | PF00134 | 0.418 |
DOC_CYCLIN_yCln2_LP_2 | 1297 | 1303 | PF00134 | 0.650 |
DOC_CYCLIN_yCln2_LP_2 | 720 | 723 | PF00134 | 0.409 |
DOC_CYCLIN_yCln2_LP_2 | 968 | 974 | PF00134 | 0.459 |
DOC_MAPK_gen_1 | 1216 | 1224 | PF00069 | 0.655 |
DOC_MAPK_gen_1 | 1289 | 1296 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 703 | 713 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 1276 | 1283 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 1289 | 1298 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 166 | 173 | PF00069 | 0.525 |
DOC_MIT_MIM_1 | 794 | 803 | PF04212 | 0.346 |
DOC_PP1_RVXF_1 | 707 | 714 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 142 | 145 | PF13499 | 0.559 |
DOC_PP2B_LxvP_1 | 147 | 150 | PF13499 | 0.549 |
DOC_PP2B_LxvP_1 | 273 | 276 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 720 | 723 | PF13499 | 0.409 |
DOC_PP2B_LxvP_1 | 968 | 971 | PF13499 | 0.471 |
DOC_PP4_FxxP_1 | 873 | 876 | PF00568 | 0.546 |
DOC_USP7_MATH_1 | 1136 | 1140 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 1206 | 1210 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 679 | 683 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 874 | 878 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.466 |
DOC_WW_Pin1_4 | 1034 | 1039 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 1125 | 1130 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 1192 | 1197 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 1249 | 1254 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 867 | 872 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 923 | 928 | PF00397 | 0.374 |
LIG_14-3-3_CanoR_1 | 1080 | 1086 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 799 | 807 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 886 | 892 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 903 | 910 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 991 | 998 | PF00244 | 0.723 |
LIG_APCC_ABBA_1 | 751 | 756 | PF00400 | 0.418 |
LIG_BIR_III_4 | 253 | 257 | PF00653 | 0.450 |
LIG_BIR_III_4 | 395 | 399 | PF00653 | 0.591 |
LIG_BRCT_BRCA1_1 | 1133 | 1137 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 419 | 423 | PF00533 | 0.384 |
LIG_BRCT_BRCA1_1 | 46 | 50 | PF00533 | 0.462 |
LIG_BRCT_BRCA1_1 | 80 | 84 | PF00533 | 0.524 |
LIG_BRCT_BRCA1_1 | 869 | 873 | PF00533 | 0.462 |
LIG_Clathr_ClatBox_1 | 49 | 53 | PF01394 | 0.414 |
LIG_Clathr_ClatBox_1 | 979 | 983 | PF01394 | 0.625 |
LIG_eIF4E_1 | 246 | 252 | PF01652 | 0.457 |
LIG_eIF4E_1 | 770 | 776 | PF01652 | 0.374 |
LIG_FHA_1 | 1210 | 1216 | PF00498 | 0.738 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.563 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.444 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.445 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.468 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.454 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.490 |
LIG_FHA_2 | 1082 | 1088 | PF00498 | 0.546 |
LIG_FHA_2 | 1089 | 1095 | PF00498 | 0.546 |
LIG_FHA_2 | 1117 | 1123 | PF00498 | 0.546 |
LIG_FHA_2 | 1250 | 1256 | PF00498 | 0.712 |
LIG_FHA_2 | 1269 | 1275 | PF00498 | 0.599 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.497 |
LIG_FHA_2 | 927 | 933 | PF00498 | 0.397 |
LIG_FHA_2 | 942 | 948 | PF00498 | 0.378 |
LIG_GSK3_LRP6_1 | 1249 | 1254 | PF00069 | 0.678 |
LIG_LIR_Apic_2 | 194 | 199 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 243 | 248 | PF02991 | 0.441 |
LIG_LIR_Apic_2 | 585 | 591 | PF02991 | 0.487 |
LIG_LIR_Apic_2 | 867 | 871 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 1084 | 1093 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 1109 | 1118 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 1154 | 1164 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 324 | 332 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 798 | 808 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 81 | 92 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 947 | 956 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 1049 | 1054 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 1084 | 1088 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 1109 | 1114 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 1134 | 1140 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 1154 | 1160 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 342 | 346 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 732 | 738 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 746 | 751 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 752 | 757 | PF02991 | 0.183 |
LIG_LIR_Nem_3 | 798 | 803 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 947 | 952 | PF02991 | 0.411 |
LIG_LYPXL_S_1 | 753 | 757 | PF13949 | 0.546 |
LIG_LYPXL_yS_3 | 754 | 757 | PF13949 | 0.346 |
LIG_MYND_1 | 145 | 149 | PF01753 | 0.617 |
LIG_MYND_1 | 471 | 475 | PF01753 | 0.538 |
LIG_NRBOX | 1293 | 1299 | PF00104 | 0.577 |
LIG_NRBOX | 420 | 426 | PF00104 | 0.451 |
LIG_PCNA_yPIPBox_3 | 1105 | 1116 | PF02747 | 0.574 |
LIG_Pex14_1 | 1079 | 1083 | PF04695 | 0.546 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.434 |
LIG_SH2_CRK | 565 | 569 | PF00017 | 0.459 |
LIG_SH2_CRK | 588 | 592 | PF00017 | 0.498 |
LIG_SH2_CRK | 748 | 752 | PF00017 | 0.346 |
LIG_SH2_CRK | 868 | 872 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 1157 | 1161 | PF00017 | 0.546 |
LIG_SH2_NCK_1 | 446 | 450 | PF00017 | 0.326 |
LIG_SH2_SRC | 1111 | 1114 | PF00017 | 0.545 |
LIG_SH2_SRC | 1131 | 1134 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 807 | 811 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 438 | 441 | PF00017 | 0.386 |
LIG_SH2_STAT3 | 879 | 882 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 1111 | 1114 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 1143 | 1146 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 1191 | 1194 | PF00017 | 0.714 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 767 | 770 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 795 | 798 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 816 | 819 | PF00017 | 0.555 |
LIG_SH3_3 | 1190 | 1196 | PF00018 | 0.719 |
LIG_SH3_3 | 1247 | 1253 | PF00018 | 0.707 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.629 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.382 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.587 |
LIG_SH3_3 | 692 | 698 | PF00018 | 0.462 |
LIG_SH3_3 | 968 | 974 | PF00018 | 0.476 |
LIG_SH3_CIN85_PxpxPR_1 | 876 | 881 | PF14604 | 0.486 |
LIG_SUMO_SIM_anti_2 | 1218 | 1223 | PF11976 | 0.648 |
LIG_SUMO_SIM_anti_2 | 1274 | 1281 | PF11976 | 0.587 |
LIG_SUMO_SIM_anti_2 | 328 | 333 | PF11976 | 0.374 |
LIG_SUMO_SIM_par_1 | 1220 | 1227 | PF11976 | 0.677 |
LIG_SUMO_SIM_par_1 | 1279 | 1285 | PF11976 | 0.576 |
LIG_SUMO_SIM_par_1 | 236 | 243 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 772 | 778 | PF11976 | 0.418 |
LIG_SUMO_SIM_par_1 | 980 | 986 | PF11976 | 0.626 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.480 |
LIG_TYR_ITIM | 341 | 346 | PF00017 | 0.529 |
LIG_WW_2 | 145 | 148 | PF00397 | 0.770 |
MOD_CK1_1 | 1081 | 1087 | PF00069 | 0.471 |
MOD_CK1_1 | 1202 | 1208 | PF00069 | 0.704 |
MOD_CK1_1 | 1209 | 1215 | PF00069 | 0.597 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.763 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.575 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.761 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.568 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.623 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.747 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.814 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.704 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.704 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.695 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.756 |
MOD_CK1_1 | 798 | 804 | PF00069 | 0.411 |
MOD_CK1_1 | 842 | 848 | PF00069 | 0.690 |
MOD_CK1_1 | 888 | 894 | PF00069 | 0.764 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.612 |
MOD_CK2_1 | 1081 | 1087 | PF00069 | 0.406 |
MOD_CK2_1 | 1088 | 1094 | PF00069 | 0.419 |
MOD_CK2_1 | 1180 | 1186 | PF00069 | 0.411 |
MOD_CK2_1 | 1249 | 1255 | PF00069 | 0.652 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.623 |
MOD_CK2_1 | 598 | 604 | PF00069 | 0.513 |
MOD_CK2_1 | 926 | 932 | PF00069 | 0.475 |
MOD_CK2_1 | 941 | 947 | PF00069 | 0.467 |
MOD_Cter_Amidation | 644 | 647 | PF01082 | 0.747 |
MOD_GlcNHglycan | 1004 | 1007 | PF01048 | 0.726 |
MOD_GlcNHglycan | 1008 | 1011 | PF01048 | 0.759 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.709 |
MOD_GlcNHglycan | 1025 | 1028 | PF01048 | 0.607 |
MOD_GlcNHglycan | 1203 | 1207 | PF01048 | 0.706 |
MOD_GlcNHglycan | 1226 | 1229 | PF01048 | 0.637 |
MOD_GlcNHglycan | 1237 | 1240 | PF01048 | 0.698 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.755 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.777 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.764 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.623 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.706 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.778 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.818 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.730 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.726 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.714 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.476 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.581 |
MOD_GlcNHglycan | 484 | 488 | PF01048 | 0.732 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.696 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.539 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.513 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.572 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.703 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.758 |
MOD_GlcNHglycan | 669 | 672 | PF01048 | 0.617 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.673 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.661 |
MOD_GlcNHglycan | 800 | 803 | PF01048 | 0.411 |
MOD_GlcNHglycan | 828 | 831 | PF01048 | 0.699 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.675 |
MOD_GlcNHglycan | 876 | 879 | PF01048 | 0.721 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.562 |
MOD_GSK3_1 | 1002 | 1009 | PF00069 | 0.690 |
MOD_GSK3_1 | 1019 | 1026 | PF00069 | 0.694 |
MOD_GSK3_1 | 1074 | 1081 | PF00069 | 0.408 |
MOD_GSK3_1 | 1178 | 1185 | PF00069 | 0.404 |
MOD_GSK3_1 | 1191 | 1198 | PF00069 | 0.688 |
MOD_GSK3_1 | 1202 | 1209 | PF00069 | 0.678 |
MOD_GSK3_1 | 1220 | 1227 | PF00069 | 0.509 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.752 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.723 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.644 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.665 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.600 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.773 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.723 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.809 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.684 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.559 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.724 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.781 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.625 |
MOD_GSK3_1 | 839 | 846 | PF00069 | 0.758 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.699 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.753 |
MOD_N-GLC_1 | 591 | 596 | PF02516 | 0.580 |
MOD_N-GLC_1 | 825 | 830 | PF02516 | 0.592 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.682 |
MOD_NEK2_1 | 1002 | 1007 | PF00069 | 0.747 |
MOD_NEK2_1 | 1078 | 1083 | PF00069 | 0.411 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.521 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.703 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.466 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.502 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.641 |
MOD_NEK2_1 | 715 | 720 | PF00069 | 0.502 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.411 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.725 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.385 |
MOD_NEK2_1 | 839 | 844 | PF00069 | 0.742 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.595 |
MOD_NEK2_2 | 621 | 626 | PF00069 | 0.683 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.764 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.772 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.693 |
MOD_PIKK_1 | 522 | 528 | PF00454 | 0.650 |
MOD_PKA_2 | 1081 | 1087 | PF00069 | 0.512 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.551 |
MOD_PKA_2 | 699 | 705 | PF00069 | 0.579 |
MOD_PKA_2 | 798 | 804 | PF00069 | 0.411 |
MOD_PKA_2 | 840 | 846 | PF00069 | 0.717 |
MOD_PKA_2 | 885 | 891 | PF00069 | 0.641 |
MOD_PKB_1 | 901 | 909 | PF00069 | 0.517 |
MOD_Plk_1 | 1153 | 1159 | PF00069 | 0.512 |
MOD_Plk_1 | 1206 | 1212 | PF00069 | 0.645 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.724 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.485 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.686 |
MOD_Plk_1 | 888 | 894 | PF00069 | 0.598 |
MOD_Plk_2-3 | 1153 | 1159 | PF00069 | 0.512 |
MOD_Plk_2-3 | 1220 | 1226 | PF00069 | 0.591 |
MOD_Plk_4 | 1074 | 1080 | PF00069 | 0.515 |
MOD_Plk_4 | 1099 | 1105 | PF00069 | 0.411 |
MOD_Plk_4 | 1206 | 1212 | PF00069 | 0.645 |
MOD_Plk_4 | 1220 | 1226 | PF00069 | 0.591 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.636 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.585 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.430 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.513 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.411 |
MOD_Plk_4 | 743 | 749 | PF00069 | 0.411 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.686 |
MOD_Plk_4 | 975 | 981 | PF00069 | 0.574 |
MOD_ProDKin_1 | 1034 | 1040 | PF00069 | 0.743 |
MOD_ProDKin_1 | 1125 | 1131 | PF00069 | 0.411 |
MOD_ProDKin_1 | 1192 | 1198 | PF00069 | 0.665 |
MOD_ProDKin_1 | 1249 | 1255 | PF00069 | 0.649 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.761 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.830 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.749 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.788 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.637 |
MOD_ProDKin_1 | 867 | 873 | PF00069 | 0.575 |
MOD_ProDKin_1 | 923 | 929 | PF00069 | 0.458 |
MOD_SUMO_for_1 | 1215 | 1218 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 402 | 409 | PF00179 | 0.667 |
TRG_DiLeu_BaEn_1 | 1275 | 1280 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_1 | 947 | 952 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 577 | 582 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 644 | 649 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 771 | 776 | PF01217 | 0.512 |
TRG_ENDOCYTIC_2 | 1051 | 1054 | PF00928 | 0.614 |
TRG_ENDOCYTIC_2 | 1111 | 1114 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 1157 | 1160 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 735 | 738 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 747 | 750 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 754 | 757 | PF00928 | 0.224 |
TRG_ER_diArg_1 | 1051 | 1053 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 1079 | 1082 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 1164 | 1166 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 629 | 632 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 646 | 648 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 707 | 709 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 901 | 904 | PF00400 | 0.530 |
TRG_NES_CRM1_1 | 1214 | 1226 | PF08389 | 0.572 |
TRG_NES_CRM1_1 | 320 | 334 | PF08389 | 0.596 |
TRG_NES_CRM1_1 | 794 | 809 | PF08389 | 0.411 |
TRG_NLS_MonoCore_2 | 705 | 710 | PF00514 | 0.521 |
TRG_NLS_MonoExtN_4 | 703 | 710 | PF00514 | 0.536 |
TRG_Pf-PMV_PEXEL_1 | 118 | 123 | PF00026 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 580 | 584 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 647 | 652 | PF00026 | 0.704 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA38 | Leptomonas seymouri | 53% | 100% |
A0A3S7WUZ0 | Leishmania donovani | 100% | 100% |
A4H9H5 | Leishmania braziliensis | 73% | 98% |
E9ARK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
Q4QDX6 | Leishmania major | 91% | 100% |