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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0070390 | transcription export complex 2 | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4I0S9
Term | Name | Level | Count |
---|---|---|---|
GO:0006405 | RNA export from nucleus | 5 | 6 |
GO:0006406 | mRNA export from nucleus | 6 | 6 |
GO:0006810 | transport | 3 | 6 |
GO:0006913 | nucleocytoplasmic transport | 5 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0015931 | nucleobase-containing compound transport | 5 | 6 |
GO:0016973 | poly(A)+ mRNA export from nucleus | 7 | 6 |
GO:0046907 | intracellular transport | 3 | 6 |
GO:0050657 | nucleic acid transport | 6 | 6 |
GO:0050658 | RNA transport | 4 | 6 |
GO:0051028 | mRNA transport | 5 | 6 |
GO:0051168 | nuclear export | 6 | 6 |
GO:0051169 | nuclear transport | 4 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
GO:0051236 | establishment of RNA localization | 3 | 6 |
GO:0051641 | cellular localization | 2 | 6 |
GO:0051649 | establishment of localization in cell | 3 | 6 |
GO:0071702 | organic substance transport | 4 | 6 |
GO:0071705 | nitrogen compound transport | 4 | 6 |
GO:0000972 | transcription-dependent tethering of RNA polymerase II gene DNA at nuclear periphery | 6 | 1 |
GO:0000973 | post-transcriptional tethering of RNA polymerase II gene DNA at nuclear periphery | 7 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006354 | DNA-templated transcription elongation | 6 | 1 |
GO:0006368 | transcription elongation by RNA polymerase II | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1146 | 1150 | PF00656 | 0.396 |
CLV_C14_Caspase3-7 | 1207 | 1211 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 1249 | 1253 | PF00656 | 0.467 |
CLV_C14_Caspase3-7 | 668 | 672 | PF00656 | 0.658 |
CLV_NRD_NRD_1 | 1064 | 1066 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 1102 | 1104 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.847 |
CLV_NRD_NRD_1 | 953 | 955 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 987 | 989 | PF00675 | 0.476 |
CLV_PCSK_KEX2_1 | 1064 | 1066 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 1102 | 1104 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 680 | 682 | PF00082 | 0.801 |
CLV_PCSK_KEX2_1 | 953 | 955 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 987 | 989 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 1005 | 1009 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 1058 | 1062 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 1102 | 1106 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 1174 | 1178 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 775 | 779 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 956 | 960 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 987 | 991 | PF00082 | 0.495 |
CLV_Separin_Metazoa | 1197 | 1201 | PF03568 | 0.471 |
DEG_APCC_DBOX_1 | 1102 | 1110 | PF00400 | 0.441 |
DEG_APCC_DBOX_1 | 1171 | 1179 | PF00400 | 0.441 |
DEG_APCC_DBOX_1 | 27 | 35 | PF00400 | 0.449 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.459 |
DEG_SCF_FBW7_1 | 323 | 330 | PF00400 | 0.659 |
DEG_SCF_FBW7_1 | 385 | 392 | PF00400 | 0.667 |
DEG_SCF_FBW7_1 | 511 | 516 | PF00400 | 0.620 |
DEG_SCF_FBW7_1 | 566 | 573 | PF00400 | 0.578 |
DEG_SPOP_SBC_1 | 322 | 326 | PF00917 | 0.658 |
DEG_SPOP_SBC_1 | 423 | 427 | PF00917 | 0.578 |
DEG_SPOP_SBC_1 | 736 | 740 | PF00917 | 0.585 |
DEG_SPOP_SBC_1 | 889 | 893 | PF00917 | 0.650 |
DOC_CDC14_PxL_1 | 781 | 789 | PF14671 | 0.445 |
DOC_CKS1_1 | 329 | 334 | PF01111 | 0.650 |
DOC_CKS1_1 | 386 | 391 | PF01111 | 0.670 |
DOC_CKS1_1 | 94 | 99 | PF01111 | 0.571 |
DOC_CKS1_1 | 997 | 1002 | PF01111 | 0.537 |
DOC_CYCLIN_RxL_1 | 1002 | 1012 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 22 | 36 | PF00134 | 0.449 |
DOC_CYCLIN_yCln2_LP_2 | 1070 | 1076 | PF00134 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 26 | 32 | PF00134 | 0.449 |
DOC_MAPK_DCC_7 | 22 | 32 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 1102 | 1109 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 1172 | 1181 | PF00069 | 0.440 |
DOC_MAPK_gen_1 | 772 | 781 | PF00069 | 0.501 |
DOC_MAPK_JIP1_4 | 28 | 34 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 1036 | 1044 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 1102 | 1109 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 1172 | 1179 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 28 | 37 | PF00069 | 0.449 |
DOC_MAPK_NFAT4_5 | 1172 | 1180 | PF00069 | 0.441 |
DOC_PP2B_LxvP_1 | 1128 | 1131 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 222 | 225 | PF13499 | 0.645 |
DOC_PP2B_LxvP_1 | 300 | 303 | PF13499 | 0.588 |
DOC_PP2B_LxvP_1 | 723 | 726 | PF13499 | 0.632 |
DOC_PP2B_LxvP_1 | 755 | 758 | PF13499 | 0.601 |
DOC_PP4_FxxP_1 | 239 | 242 | PF00568 | 0.586 |
DOC_PP4_FxxP_1 | 271 | 274 | PF00568 | 0.701 |
DOC_PP4_FxxP_1 | 543 | 546 | PF00568 | 0.699 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 424 | 428 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 615 | 619 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 705 | 709 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 714 | 718 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 735 | 739 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 794 | 798 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 889 | 893 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 894 | 898 | PF00917 | 0.571 |
DOC_WW_Pin1_4 | 1237 | 1242 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 559 | 564 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 636 | 641 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 683 | 688 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 712 | 717 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 996 | 1001 | PF00397 | 0.565 |
LIG_14-3-3_CanoR_1 | 1005 | 1011 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 1075 | 1079 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 1192 | 1201 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 1203 | 1213 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 266 | 272 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 681 | 687 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 772 | 778 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 953 | 959 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 965 | 971 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 987 | 997 | PF00244 | 0.567 |
LIG_APCC_ABBA_1 | 348 | 353 | PF00400 | 0.607 |
LIG_BIR_III_2 | 1243 | 1247 | PF00653 | 0.472 |
LIG_BIR_III_2 | 941 | 945 | PF00653 | 0.508 |
LIG_BIR_III_4 | 393 | 397 | PF00653 | 0.711 |
LIG_BIR_III_4 | 85 | 89 | PF00653 | 0.547 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.726 |
LIG_BRCT_BRCA1_1 | 488 | 492 | PF00533 | 0.688 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 662 | 666 | PF00533 | 0.628 |
LIG_BRCT_BRCA1_1 | 978 | 982 | PF00533 | 0.456 |
LIG_deltaCOP1_diTrp_1 | 861 | 867 | PF00928 | 0.450 |
LIG_EH1_1 | 1023 | 1031 | PF00400 | 0.425 |
LIG_EVH1_1 | 755 | 759 | PF00568 | 0.553 |
LIG_FHA_1 | 1132 | 1138 | PF00498 | 0.441 |
LIG_FHA_1 | 1140 | 1146 | PF00498 | 0.421 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.633 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.639 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.774 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.710 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.616 |
LIG_FHA_1 | 911 | 917 | PF00498 | 0.498 |
LIG_FHA_1 | 976 | 982 | PF00498 | 0.523 |
LIG_FHA_1 | 989 | 995 | PF00498 | 0.381 |
LIG_FHA_2 | 1238 | 1244 | PF00498 | 0.446 |
LIG_FHA_2 | 1247 | 1253 | PF00498 | 0.376 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.461 |
LIG_FHA_2 | 825 | 831 | PF00498 | 0.581 |
LIG_FHA_2 | 997 | 1003 | PF00498 | 0.537 |
LIG_GBD_Chelix_1 | 1106 | 1114 | PF00786 | 0.424 |
LIG_HCF-1_HBM_1 | 1230 | 1233 | PF13415 | 0.494 |
LIG_IRF3_LxIS_1 | 1040 | 1045 | PF10401 | 0.447 |
LIG_LIR_Apic_2 | 270 | 274 | PF02991 | 0.693 |
LIG_LIR_Apic_2 | 541 | 546 | PF02991 | 0.701 |
LIG_LIR_Gen_1 | 1021 | 1032 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 1122 | 1133 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 1230 | 1241 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 401 | 408 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 861 | 869 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 979 | 989 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 1021 | 1027 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 1122 | 1128 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 1230 | 1236 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 1240 | 1245 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 134 | 138 | PF02991 | 0.682 |
LIG_LIR_Nem_3 | 401 | 406 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 534 | 539 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 68 | 72 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 808 | 814 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 861 | 866 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 979 | 985 | PF02991 | 0.467 |
LIG_MYND_1 | 378 | 382 | PF01753 | 0.650 |
LIG_MYND_1 | 420 | 424 | PF01753 | 0.659 |
LIG_NRBOX | 1105 | 1111 | PF00104 | 0.423 |
LIG_NRBOX | 30 | 36 | PF00104 | 0.475 |
LIG_NRBOX | 925 | 931 | PF00104 | 0.455 |
LIG_OCRL_FandH_1 | 535 | 547 | PF00620 | 0.650 |
LIG_Pex14_1 | 1006 | 1010 | PF04695 | 0.497 |
LIG_Pex14_1 | 863 | 867 | PF04695 | 0.441 |
LIG_Pex14_2 | 1043 | 1047 | PF04695 | 0.434 |
LIG_Pex14_2 | 56 | 60 | PF04695 | 0.495 |
LIG_RPA_C_Fungi | 1060 | 1072 | PF08784 | 0.388 |
LIG_SH2_CRK | 1201 | 1205 | PF00017 | 0.483 |
LIG_SH2_CRK | 945 | 949 | PF00017 | 0.468 |
LIG_SH2_GRB2like | 872 | 875 | PF00017 | 0.448 |
LIG_SH2_GRB2like | 922 | 925 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 1206 | 1210 | PF00017 | 0.473 |
LIG_SH2_NCK_1 | 945 | 949 | PF00017 | 0.468 |
LIG_SH2_SRC | 1024 | 1027 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 922 | 926 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 1024 | 1027 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 1184 | 1187 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 1233 | 1236 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 872 | 875 | PF00017 | 0.448 |
LIG_SH3_1 | 346 | 352 | PF00018 | 0.642 |
LIG_SH3_1 | 656 | 662 | PF00018 | 0.604 |
LIG_SH3_2 | 659 | 664 | PF14604 | 0.611 |
LIG_SH3_3 | 1088 | 1094 | PF00018 | 0.549 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.676 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.680 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.474 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.647 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.768 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.638 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.526 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.441 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.791 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.803 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.726 |
LIG_SH3_3 | 560 | 566 | PF00018 | 0.656 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.709 |
LIG_SH3_3 | 638 | 644 | PF00018 | 0.624 |
LIG_SH3_3 | 654 | 660 | PF00018 | 0.538 |
LIG_SH3_3 | 699 | 705 | PF00018 | 0.732 |
LIG_SH3_3 | 753 | 759 | PF00018 | 0.569 |
LIG_SUMO_SIM_anti_2 | 1142 | 1149 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 1217 | 1222 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 30 | 36 | PF11976 | 0.475 |
LIG_TRAF2_1 | 798 | 801 | PF00917 | 0.608 |
LIG_TYR_ITIM | 1199 | 1204 | PF00017 | 0.477 |
LIG_UBA3_1 | 1216 | 1223 | PF00899 | 0.465 |
LIG_UBA3_1 | 876 | 884 | PF00899 | 0.504 |
LIG_UBA3_1 | 981 | 990 | PF00899 | 0.468 |
LIG_WRC_WIRS_1 | 1019 | 1024 | PF05994 | 0.426 |
LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.538 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.628 |
LIG_WW_2 | 420 | 423 | PF00397 | 0.639 |
LIG_WW_2 | 758 | 761 | PF00397 | 0.576 |
MOD_CDK_SPK_2 | 341 | 346 | PF00069 | 0.580 |
MOD_CDK_SPK_2 | 683 | 688 | PF00069 | 0.599 |
MOD_CDK_SPxK_1 | 636 | 642 | PF00069 | 0.653 |
MOD_CDK_SPxxK_3 | 446 | 453 | PF00069 | 0.578 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.642 |
MOD_CK1_1 | 1191 | 1197 | PF00069 | 0.413 |
MOD_CK1_1 | 1237 | 1243 | PF00069 | 0.438 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.685 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.630 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.700 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.689 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.675 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.703 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.592 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.588 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.685 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.776 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.651 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.526 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.697 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.680 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.686 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.684 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.536 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.594 |
MOD_CK1_1 | 844 | 850 | PF00069 | 0.500 |
MOD_CK1_1 | 882 | 888 | PF00069 | 0.596 |
MOD_CK1_1 | 892 | 898 | PF00069 | 0.521 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.550 |
MOD_CK2_1 | 1074 | 1080 | PF00069 | 0.472 |
MOD_CK2_1 | 1191 | 1197 | PF00069 | 0.413 |
MOD_CK2_1 | 718 | 724 | PF00069 | 0.650 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.685 |
MOD_CK2_1 | 824 | 830 | PF00069 | 0.513 |
MOD_CK2_1 | 996 | 1002 | PF00069 | 0.562 |
MOD_Cter_Amidation | 678 | 681 | PF01082 | 0.735 |
MOD_DYRK1A_RPxSP_1 | 50 | 54 | PF00069 | 0.510 |
MOD_GlcNHglycan | 1044 | 1047 | PF01048 | 0.454 |
MOD_GlcNHglycan | 1052 | 1055 | PF01048 | 0.422 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.611 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.587 |
MOD_GlcNHglycan | 1206 | 1209 | PF01048 | 0.381 |
MOD_GlcNHglycan | 1236 | 1239 | PF01048 | 0.522 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.726 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.596 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.549 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.712 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.697 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.759 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.723 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.649 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.776 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.779 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.653 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.624 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.711 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.674 |
MOD_GlcNHglycan | 407 | 411 | PF01048 | 0.638 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.677 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.687 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.628 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.722 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.577 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.644 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.644 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.572 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.698 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.630 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.570 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.578 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.707 |
MOD_GlcNHglycan | 693 | 699 | PF01048 | 0.811 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.656 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.677 |
MOD_GlcNHglycan | 782 | 785 | PF01048 | 0.567 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.670 |
MOD_GlcNHglycan | 855 | 858 | PF01048 | 0.554 |
MOD_GlcNHglycan | 884 | 887 | PF01048 | 0.597 |
MOD_GlcNHglycan | 892 | 895 | PF01048 | 0.533 |
MOD_GlcNHglycan | 991 | 994 | PF01048 | 0.497 |
MOD_GSK3_1 | 1014 | 1021 | PF00069 | 0.395 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.667 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.637 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.666 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.543 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.723 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.687 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.755 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.692 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.652 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.649 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.638 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.679 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.659 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.689 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.701 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.699 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.604 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.807 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.656 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.675 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.609 |
MOD_GSK3_1 | 868 | 875 | PF00069 | 0.504 |
MOD_GSK3_1 | 876 | 883 | PF00069 | 0.480 |
MOD_GSK3_1 | 888 | 895 | PF00069 | 0.469 |
MOD_GSK3_1 | 910 | 917 | PF00069 | 0.456 |
MOD_GSK3_1 | 969 | 976 | PF00069 | 0.619 |
MOD_N-GLC_1 | 1095 | 1100 | PF02516 | 0.365 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.693 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.645 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.675 |
MOD_N-GLC_1 | 529 | 534 | PF02516 | 0.700 |
MOD_NEK2_1 | 1018 | 1023 | PF00069 | 0.423 |
MOD_NEK2_1 | 1042 | 1047 | PF00069 | 0.437 |
MOD_NEK2_1 | 1074 | 1079 | PF00069 | 0.471 |
MOD_NEK2_1 | 1140 | 1145 | PF00069 | 0.423 |
MOD_NEK2_1 | 1183 | 1188 | PF00069 | 0.581 |
MOD_NEK2_1 | 1234 | 1239 | PF00069 | 0.475 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.641 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.503 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.603 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.665 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.446 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.742 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.750 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.749 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.504 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.721 |
MOD_NEK2_1 | 710 | 715 | PF00069 | 0.795 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.514 |
MOD_NEK2_1 | 880 | 885 | PF00069 | 0.497 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.476 |
MOD_NEK2_1 | 929 | 934 | PF00069 | 0.345 |
MOD_NEK2_2 | 1150 | 1155 | PF00069 | 0.343 |
MOD_NEK2_2 | 424 | 429 | PF00069 | 0.655 |
MOD_NEK2_2 | 628 | 633 | PF00069 | 0.637 |
MOD_OFUCOSY | 40 | 46 | PF10250 | 0.457 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.656 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.778 |
MOD_PIKK_1 | 739 | 745 | PF00454 | 0.659 |
MOD_PIKK_1 | 747 | 753 | PF00454 | 0.510 |
MOD_PIKK_1 | 845 | 851 | PF00454 | 0.617 |
MOD_PK_1 | 531 | 537 | PF00069 | 0.696 |
MOD_PK_1 | 954 | 960 | PF00069 | 0.458 |
MOD_PKA_2 | 1074 | 1080 | PF00069 | 0.420 |
MOD_PKA_2 | 1191 | 1197 | PF00069 | 0.524 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.779 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.683 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.660 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.650 |
MOD_PKA_2 | 845 | 851 | PF00069 | 0.668 |
MOD_PKB_1 | 680 | 688 | PF00069 | 0.772 |
MOD_Plk_1 | 1095 | 1101 | PF00069 | 0.364 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.646 |
MOD_Plk_4 | 1014 | 1020 | PF00069 | 0.397 |
MOD_Plk_4 | 1074 | 1080 | PF00069 | 0.472 |
MOD_Plk_4 | 1087 | 1093 | PF00069 | 0.332 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.651 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.739 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.709 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.476 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.686 |
MOD_Plk_4 | 773 | 779 | PF00069 | 0.509 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.444 |
MOD_Plk_4 | 929 | 935 | PF00069 | 0.355 |
MOD_Plk_4 | 943 | 949 | PF00069 | 0.477 |
MOD_ProDKin_1 | 1237 | 1243 | PF00069 | 0.438 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.634 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.661 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.525 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.749 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.561 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.670 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.669 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.609 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.485 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.737 |
MOD_ProDKin_1 | 559 | 565 | PF00069 | 0.637 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.616 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.704 |
MOD_ProDKin_1 | 636 | 642 | PF00069 | 0.653 |
MOD_ProDKin_1 | 683 | 689 | PF00069 | 0.597 |
MOD_ProDKin_1 | 712 | 718 | PF00069 | 0.700 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.571 |
MOD_ProDKin_1 | 996 | 1002 | PF00069 | 0.562 |
MOD_SUMO_rev_2 | 163 | 172 | PF00179 | 0.608 |
MOD_SUMO_rev_2 | 387 | 397 | PF00179 | 0.639 |
MOD_SUMO_rev_2 | 763 | 767 | PF00179 | 0.562 |
TRG_DiLeu_BaEn_1 | 1014 | 1019 | PF01217 | 0.451 |
TRG_DiLeu_BaEn_1 | 1081 | 1086 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_1 | 925 | 930 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 1215 | 1220 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 199 | 204 | PF01217 | 0.620 |
TRG_DiLeu_BaLyEn_6 | 26 | 31 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 79 | 84 | PF01217 | 0.634 |
TRG_ENDOCYTIC_2 | 1024 | 1027 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 1201 | 1204 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 1206 | 1209 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 1233 | 1236 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.638 |
TRG_ENDOCYTIC_2 | 945 | 948 | PF00928 | 0.469 |
TRG_ER_diArg_1 | 1063 | 1065 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 1102 | 1104 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 1172 | 1175 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 680 | 682 | PF00400 | 0.863 |
TRG_ER_diArg_1 | 952 | 954 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 987 | 989 | PF00400 | 0.476 |
TRG_NES_CRM1_1 | 1016 | 1028 | PF08389 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WY79 | Leishmania donovani | 99% | 100% |
A4HDE6 | Leishmania braziliensis | 68% | 98% |
E9AWT1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QAP3 | Leishmania major | 88% | 99% |