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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0016020 | membrane | 2 | 12 |
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 | 12 |
Related structures:
AlphaFold database: Q4QII2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 2 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 2 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019725 | cellular homeostasis | 2 | 2 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 2 |
GO:0042592 | homeostatic process | 3 | 2 |
GO:0048878 | chemical homeostasis | 4 | 2 |
GO:0050801 | monoatomic ion homeostasis | 5 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 2 |
GO:0055074 | calcium ion homeostasis | 8 | 2 |
GO:0055080 | monoatomic cation homeostasis | 6 | 2 |
GO:0055082 | intracellular chemical homeostasis | 3 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 2 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 2 |
GO:0098771 | inorganic ion homeostasis | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005215 | transporter activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 12 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 12 |
GO:0015662 | P-type ion transporter activity | 4 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 12 |
GO:0022804 | active transmembrane transporter activity | 3 | 12 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.549 |
CLV_C14_Caspase3-7 | 619 | 623 | PF00656 | 0.568 |
CLV_C14_Caspase3-7 | 667 | 671 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 759 | 763 | PF00656 | 0.600 |
CLV_NRD_NRD_1 | 1173 | 1175 | PF00675 | 0.324 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 785 | 787 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 931 | 933 | PF00675 | 0.337 |
CLV_PCSK_FUR_1 | 783 | 787 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.215 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 745 | 747 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 785 | 787 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 931 | 933 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 274 | 276 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.235 |
CLV_PCSK_PC1ET2_1 | 745 | 747 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 931 | 933 | PF00082 | 0.423 |
CLV_PCSK_PC7_1 | 16 | 22 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 1008 | 1012 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 1078 | 1082 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 1087 | 1091 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 1177 | 1181 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 705 | 709 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 937 | 941 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 944 | 948 | PF00082 | 0.342 |
DEG_APCC_DBOX_1 | 1176 | 1184 | PF00400 | 0.490 |
DEG_ODPH_VHL_1 | 788 | 799 | PF01847 | 0.550 |
DOC_CDC14_PxL_1 | 42 | 50 | PF14671 | 0.529 |
DOC_CKS1_1 | 915 | 920 | PF01111 | 0.649 |
DOC_CYCLIN_RxL_1 | 1028 | 1040 | PF00134 | 0.443 |
DOC_CYCLIN_yCln2_LP_2 | 603 | 609 | PF00134 | 0.601 |
DOC_MAPK_DCC_7 | 279 | 288 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 1174 | 1183 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 1216 | 1225 | PF00069 | 0.254 |
DOC_MAPK_gen_1 | 254 | 264 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 337 | 345 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 367 | 375 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 434 | 441 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 673 | 682 | PF00069 | 0.624 |
DOC_MAPK_HePTP_8 | 276 | 288 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 1174 | 1183 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 279 | 288 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 369 | 377 | PF00069 | 0.441 |
DOC_PP1_RVXF_1 | 687 | 694 | PF00149 | 0.496 |
DOC_PP2B_LxvP_1 | 898 | 901 | PF13499 | 0.621 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.494 |
DOC_PP4_FxxP_1 | 481 | 484 | PF00568 | 0.492 |
DOC_USP7_MATH_1 | 1009 | 1013 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 1125 | 1129 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.535 |
DOC_USP7_UBL2_3 | 1054 | 1058 | PF12436 | 0.339 |
DOC_USP7_UBL2_3 | 523 | 527 | PF12436 | 0.564 |
DOC_USP7_UBL2_3 | 704 | 708 | PF12436 | 0.501 |
DOC_USP7_UBL2_3 | 876 | 880 | PF12436 | 0.686 |
DOC_USP7_UBL2_3 | 933 | 937 | PF12436 | 0.627 |
DOC_USP7_UBL2_3 | 947 | 951 | PF12436 | 0.589 |
DOC_USP7_UBL2_3 | 953 | 957 | PF12436 | 0.577 |
DOC_WW_Pin1_4 | 1195 | 1200 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 802 | 807 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 914 | 919 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 1021 | 1025 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 1216 | 1225 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 251 | 257 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 369 | 377 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.348 |
LIG_Actin_WH2_2 | 411 | 428 | PF00022 | 0.441 |
LIG_Actin_WH2_2 | 635 | 650 | PF00022 | 0.602 |
LIG_ActinCP_TwfCPI_2 | 154 | 162 | PF01115 | 0.497 |
LIG_AP2alpha_1 | 199 | 203 | PF02296 | 0.560 |
LIG_APCC_ABBA_1 | 1238 | 1243 | PF00400 | 0.595 |
LIG_APCC_ABBA_1 | 124 | 129 | PF00400 | 0.612 |
LIG_APCC_ABBA_1 | 42 | 47 | PF00400 | 0.443 |
LIG_BIR_III_4 | 1226 | 1230 | PF00653 | 0.309 |
LIG_BIR_III_4 | 185 | 189 | PF00653 | 0.477 |
LIG_BIR_III_4 | 752 | 756 | PF00653 | 0.599 |
LIG_BRCT_BRCA1_1 | 1067 | 1071 | PF00533 | 0.309 |
LIG_BRCT_BRCA1_1 | 1145 | 1149 | PF00533 | 0.309 |
LIG_BRCT_BRCA1_1 | 208 | 212 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.495 |
LIG_Clathr_ClatBox_1 | 1222 | 1226 | PF01394 | 0.378 |
LIG_Clathr_ClatBox_1 | 283 | 287 | PF01394 | 0.441 |
LIG_Clathr_ClatBox_1 | 539 | 543 | PF01394 | 0.525 |
LIG_CtBP_PxDLS_1 | 456 | 460 | PF00389 | 0.441 |
LIG_deltaCOP1_diTrp_1 | 22 | 30 | PF00928 | 0.546 |
LIG_deltaCOP1_diTrp_1 | 225 | 233 | PF00928 | 0.241 |
LIG_eIF4E_1 | 227 | 233 | PF01652 | 0.252 |
LIG_eIF4E_1 | 43 | 49 | PF01652 | 0.430 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.668 |
LIG_FHA_1 | 1020 | 1026 | PF00498 | 0.549 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.514 |
LIG_FHA_1 | 1145 | 1151 | PF00498 | 0.335 |
LIG_FHA_1 | 1157 | 1163 | PF00498 | 0.264 |
LIG_FHA_1 | 1218 | 1224 | PF00498 | 0.390 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.578 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.441 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.430 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.463 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.441 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.440 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.372 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.474 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.362 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.552 |
LIG_FHA_1 | 850 | 856 | PF00498 | 0.548 |
LIG_FHA_2 | 1124 | 1130 | PF00498 | 0.412 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.585 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.426 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.500 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.351 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.615 |
LIG_FHA_2 | 770 | 776 | PF00498 | 0.628 |
LIG_FHA_2 | 813 | 819 | PF00498 | 0.570 |
LIG_FHA_2 | 827 | 833 | PF00498 | 0.498 |
LIG_LIR_Apic_2 | 478 | 484 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 1068 | 1079 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 1217 | 1227 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 234 | 241 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 47 | 57 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 60 | 68 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 78 | 85 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 917 | 927 | PF02991 | 0.639 |
LIG_LIR_LC3C_4 | 881 | 884 | PF02991 | 0.721 |
LIG_LIR_Nem_3 | 1090 | 1096 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 1100 | 1105 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 1217 | 1222 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 1226 | 1231 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.250 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 435 | 440 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 597 | 602 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.293 |
LIG_LYPXL_S_1 | 44 | 48 | PF13949 | 0.611 |
LIG_LYPXL_yS_3 | 45 | 48 | PF13949 | 0.411 |
LIG_MLH1_MIPbox_1 | 208 | 212 | PF16413 | 0.414 |
LIG_PCNA_yPIPBox_3 | 1085 | 1093 | PF02747 | 0.582 |
LIG_Pex14_1 | 86 | 90 | PF04695 | 0.495 |
LIG_Pex14_2 | 1215 | 1219 | PF04695 | 0.251 |
LIG_Pex14_2 | 199 | 203 | PF04695 | 0.540 |
LIG_Pex14_2 | 75 | 79 | PF04695 | 0.313 |
LIG_SH2_CRK | 1031 | 1035 | PF00017 | 0.437 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.642 |
LIG_SH2_CRK | 599 | 603 | PF00017 | 0.508 |
LIG_SH2_CRK | 658 | 662 | PF00017 | 0.520 |
LIG_SH2_CRK | 665 | 669 | PF00017 | 0.525 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.584 |
LIG_SH2_NCK_1 | 1134 | 1138 | PF00017 | 0.288 |
LIG_SH2_PTP2 | 699 | 702 | PF00017 | 0.581 |
LIG_SH2_SRC | 1134 | 1137 | PF00017 | 0.449 |
LIG_SH2_SRC | 43 | 46 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 1043 | 1047 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 528 | 532 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 1110 | 1113 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.225 |
LIG_SH2_STAT5 | 625 | 628 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 699 | 702 | PF00017 | 0.581 |
LIG_SH3_2 | 157 | 162 | PF14604 | 0.499 |
LIG_SH3_3 | 1089 | 1095 | PF00018 | 0.518 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.493 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.524 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.441 |
LIG_SH3_3 | 571 | 577 | PF00018 | 0.585 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.537 |
LIG_SH3_3 | 764 | 770 | PF00018 | 0.665 |
LIG_SH3_3 | 880 | 886 | PF00018 | 0.747 |
LIG_SH3_3 | 889 | 895 | PF00018 | 0.629 |
LIG_SH3_3 | 905 | 911 | PF00018 | 0.532 |
LIG_SH3_3 | 912 | 918 | PF00018 | 0.570 |
LIG_SH3_3 | 957 | 963 | PF00018 | 0.645 |
LIG_SUMO_SIM_anti_2 | 1220 | 1226 | PF11976 | 0.450 |
LIG_SUMO_SIM_anti_2 | 266 | 271 | PF11976 | 0.466 |
LIG_SUMO_SIM_anti_2 | 287 | 293 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 370 | 377 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 1220 | 1226 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 465 | 471 | PF11976 | 0.512 |
LIG_TRAF2_1 | 1211 | 1214 | PF00917 | 0.360 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.527 |
LIG_TYR_ITIM | 663 | 668 | PF00017 | 0.407 |
LIG_TYR_ITIM | 94 | 99 | PF00017 | 0.476 |
LIG_TYR_ITSM | 243 | 250 | PF00017 | 0.554 |
LIG_UBA3_1 | 467 | 472 | PF00899 | 0.309 |
LIG_UBA3_1 | 518 | 527 | PF00899 | 0.472 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.440 |
MOD_CDK_SPxxK_3 | 317 | 324 | PF00069 | 0.293 |
MOD_CK1_1 | 1156 | 1162 | PF00069 | 0.414 |
MOD_CK1_1 | 1195 | 1201 | PF00069 | 0.500 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.293 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.309 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.498 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.439 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.549 |
MOD_CK1_1 | 728 | 734 | PF00069 | 0.360 |
MOD_CK1_1 | 763 | 769 | PF00069 | 0.526 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.323 |
MOD_CK1_1 | 805 | 811 | PF00069 | 0.443 |
MOD_CK1_1 | 965 | 971 | PF00069 | 0.621 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.373 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.372 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.524 |
MOD_CK2_1 | 812 | 818 | PF00069 | 0.462 |
MOD_CK2_1 | 826 | 832 | PF00069 | 0.350 |
MOD_CK2_1 | 978 | 984 | PF00069 | 0.684 |
MOD_CMANNOS | 23 | 26 | PF00535 | 0.403 |
MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.409 |
MOD_Cter_Amidation | 954 | 957 | PF01082 | 0.624 |
MOD_GlcNHglycan | 1155 | 1158 | PF01048 | 0.350 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.299 |
MOD_GlcNHglycan | 401 | 405 | PF01048 | 0.308 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.183 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.412 |
MOD_GlcNHglycan | 869 | 872 | PF01048 | 0.546 |
MOD_GSK3_1 | 1004 | 1011 | PF00069 | 0.424 |
MOD_GSK3_1 | 1019 | 1026 | PF00069 | 0.236 |
MOD_GSK3_1 | 1037 | 1044 | PF00069 | 0.293 |
MOD_GSK3_1 | 1074 | 1081 | PF00069 | 0.483 |
MOD_GSK3_1 | 1139 | 1146 | PF00069 | 0.386 |
MOD_GSK3_1 | 1149 | 1156 | PF00069 | 0.293 |
MOD_GSK3_1 | 1205 | 1212 | PF00069 | 0.473 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.293 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.271 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.274 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.348 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.447 |
MOD_GSK3_1 | 974 | 981 | PF00069 | 0.700 |
MOD_LATS_1 | 365 | 371 | PF00433 | 0.392 |
MOD_N-GLC_1 | 1144 | 1149 | PF02516 | 0.414 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.309 |
MOD_N-GLC_1 | 712 | 717 | PF02516 | 0.432 |
MOD_N-GLC_1 | 965 | 970 | PF02516 | 0.645 |
MOD_NEK2_1 | 1019 | 1024 | PF00069 | 0.325 |
MOD_NEK2_1 | 1072 | 1077 | PF00069 | 0.409 |
MOD_NEK2_1 | 1097 | 1102 | PF00069 | 0.293 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.453 |
MOD_NEK2_1 | 1112 | 1117 | PF00069 | 0.347 |
MOD_NEK2_1 | 1143 | 1148 | PF00069 | 0.303 |
MOD_NEK2_1 | 1149 | 1154 | PF00069 | 0.308 |
MOD_NEK2_1 | 1205 | 1210 | PF00069 | 0.501 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.293 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.321 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.293 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.350 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.293 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.210 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.362 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.352 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.505 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.411 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.452 |
MOD_NEK2_1 | 781 | 786 | PF00069 | 0.498 |
MOD_NEK2_1 | 904 | 909 | PF00069 | 0.480 |
MOD_NEK2_1 | 974 | 979 | PF00069 | 0.531 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.293 |
MOD_PIKK_1 | 1037 | 1043 | PF00454 | 0.410 |
MOD_PIKK_1 | 1217 | 1223 | PF00454 | 0.431 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.350 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.293 |
MOD_PIKK_1 | 826 | 832 | PF00454 | 0.431 |
MOD_PKA_1 | 274 | 280 | PF00069 | 0.409 |
MOD_PKA_2 | 1020 | 1026 | PF00069 | 0.325 |
MOD_PKA_2 | 1217 | 1223 | PF00069 | 0.414 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.350 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.207 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.293 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.446 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.599 |
MOD_PKB_1 | 1085 | 1093 | PF00069 | 0.444 |
MOD_Plk_1 | 1144 | 1150 | PF00069 | 0.414 |
MOD_Plk_1 | 1205 | 1211 | PF00069 | 0.476 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.293 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.309 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.293 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.569 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.405 |
MOD_Plk_1 | 737 | 743 | PF00069 | 0.425 |
MOD_Plk_1 | 995 | 1001 | PF00069 | 0.407 |
MOD_Plk_2-3 | 1123 | 1129 | PF00069 | 0.501 |
MOD_Plk_4 | 1020 | 1026 | PF00069 | 0.323 |
MOD_Plk_4 | 1043 | 1049 | PF00069 | 0.293 |
MOD_Plk_4 | 1097 | 1103 | PF00069 | 0.293 |
MOD_Plk_4 | 1112 | 1118 | PF00069 | 0.345 |
MOD_Plk_4 | 1139 | 1145 | PF00069 | 0.363 |
MOD_Plk_4 | 1150 | 1156 | PF00069 | 0.293 |
MOD_Plk_4 | 1234 | 1240 | PF00069 | 0.470 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.305 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.293 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.293 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.296 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.374 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.144 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.386 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.381 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.409 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.566 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.466 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.425 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.323 |
MOD_Plk_4 | 763 | 769 | PF00069 | 0.614 |
MOD_Plk_4 | 818 | 824 | PF00069 | 0.447 |
MOD_Plk_4 | 974 | 980 | PF00069 | 0.519 |
MOD_ProDKin_1 | 1195 | 1201 | PF00069 | 0.500 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.414 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.293 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.401 |
MOD_ProDKin_1 | 802 | 808 | PF00069 | 0.502 |
MOD_ProDKin_1 | 914 | 920 | PF00069 | 0.549 |
MOD_SUMO_for_1 | 875 | 878 | PF00179 | 0.730 |
MOD_SUMO_rev_2 | 1135 | 1142 | PF00179 | 0.445 |
MOD_SUMO_rev_2 | 511 | 518 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 567 | 577 | PF00179 | 0.603 |
MOD_SUMO_rev_2 | 619 | 626 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 685 | 691 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 872 | 882 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 891 | 901 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 929 | 939 | PF00179 | 0.581 |
TRG_DiLeu_BaEn_1 | 1234 | 1239 | PF01217 | 0.470 |
TRG_DiLeu_BaEn_1 | 878 | 883 | PF01217 | 0.678 |
TRG_DiLeu_BaEn_2 | 404 | 410 | PF01217 | 0.293 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 1031 | 1034 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 1110 | 1113 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 1134 | 1137 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 665 | 668 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.488 |
TRG_ER_diArg_1 | 1085 | 1088 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 1215 | 1218 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 611 | 613 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 682 | 684 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 783 | 786 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 90 | 93 | PF00400 | 0.514 |
TRG_NES_CRM1_1 | 102 | 113 | PF08389 | 0.287 |
TRG_NLS_MonoExtC_3 | 1173 | 1178 | PF00514 | 0.418 |
TRG_NLS_MonoExtC_3 | 142 | 148 | PF00514 | 0.415 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.270 |
TRG_Pf-PMV_PEXEL_1 | 666 | 670 | PF00026 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 944 | 948 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZI4 | Leptomonas seymouri | 82% | 100% |
A0A0S4INU6 | Bodo saltans | 57% | 100% |
A0A1X0NPJ3 | Trypanosomatidae | 66% | 100% |
A0A3R7N8T2 | Trypanosoma rangeli | 67% | 100% |
A0A3S5H614 | Leishmania donovani | 96% | 100% |
A0A451EJU6 | Leishmania donovani | 21% | 100% |
A4H3S2 | Leishmania braziliensis | 21% | 100% |
A4H553 | Leishmania braziliensis | 89% | 100% |
A4HRZ6 | Leishmania infantum | 21% | 100% |
A4HTD0 | Leishmania infantum | 96% | 100% |
C9ZUI4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 99% |
E9ALC3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O14072 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
P39986 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
Q9LT02 | Arabidopsis thaliana | 35% | 100% |
V5BNZ8 | Trypanosoma cruzi | 67% | 100% |