Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 1 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 6 |
Forrest at al. (procyclic) | no | yes: 6 |
Silverman et al. | no | yes: 4 |
Pissara et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 25 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 25 |
GO:0110165 | cellular anatomical entity | 1 | 26 |
GO:0016020 | membrane | 2 | 1 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 4 |
Related structures:
AlphaFold database: A0A3Q8ICR2
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 4 |
GO:0006458 | 'de novo' protein folding | 3 | 4 |
GO:0006950 | response to stress | 2 | 4 |
GO:0006986 | response to unfolded protein | 4 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0010033 | response to organic substance | 3 | 4 |
GO:0033554 | cellular response to stress | 3 | 4 |
GO:0034620 | cellular response to unfolded protein | 5 | 4 |
GO:0035966 | response to topologically incorrect protein | 3 | 4 |
GO:0035967 | cellular response to topologically incorrect protein | 4 | 4 |
GO:0042026 | protein refolding | 3 | 4 |
GO:0042221 | response to chemical | 2 | 4 |
GO:0050896 | response to stimulus | 1 | 4 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 4 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 4 |
GO:0051716 | cellular response to stimulus | 2 | 4 |
GO:0061077 | chaperone-mediated protein folding | 3 | 4 |
GO:0070887 | cellular response to chemical stimulus | 3 | 4 |
GO:0071310 | cellular response to organic substance | 4 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 26 |
GO:0005488 | binding | 1 | 26 |
GO:0005524 | ATP binding | 5 | 26 |
GO:0017076 | purine nucleotide binding | 4 | 26 |
GO:0030554 | adenyl nucleotide binding | 5 | 26 |
GO:0032553 | ribonucleotide binding | 3 | 26 |
GO:0032555 | purine ribonucleotide binding | 4 | 26 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 26 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 26 |
GO:0036094 | small molecule binding | 2 | 26 |
GO:0043167 | ion binding | 2 | 26 |
GO:0043168 | anion binding | 3 | 26 |
GO:0044183 | protein folding chaperone | 1 | 26 |
GO:0097159 | organic cyclic compound binding | 2 | 26 |
GO:0097367 | carbohydrate derivative binding | 2 | 26 |
GO:0140657 | ATP-dependent activity | 1 | 26 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 26 |
GO:1901265 | nucleoside phosphate binding | 3 | 26 |
GO:1901363 | heterocyclic compound binding | 2 | 26 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0005515 | protein binding | 2 | 4 |
GO:0016462 | pyrophosphatase activity | 5 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 4 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 4 |
GO:0016887 | ATP hydrolysis activity | 7 | 4 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 4 |
GO:0031072 | heat shock protein binding | 3 | 4 |
GO:0051082 | unfolded protein binding | 3 | 4 |
GO:0051787 | misfolded protein binding | 3 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.373 |
CLV_C14_Caspase3-7 | 688 | 692 | PF00656 | 0.497 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 775 | 777 | PF00675 | 0.549 |
CLV_PCSK_FUR_1 | 276 | 280 | PF00082 | 0.327 |
CLV_PCSK_FUR_1 | 85 | 89 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 774 | 776 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 887 | 889 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.356 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 650 | 652 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 887 | 889 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 855 | 859 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 867 | 871 | PF00082 | 0.447 |
CLV_Separin_Metazoa | 675 | 679 | PF03568 | 0.386 |
DEG_APCC_DBOX_1 | 854 | 862 | PF00400 | 0.530 |
DEG_SPOP_SBC_1 | 304 | 308 | PF00917 | 0.666 |
DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.545 |
DOC_CKS1_1 | 237 | 242 | PF01111 | 0.232 |
DOC_CYCLIN_RxL_1 | 333 | 342 | PF00134 | 0.233 |
DOC_CYCLIN_RxL_1 | 410 | 420 | PF00134 | 0.232 |
DOC_CYCLIN_RxL_1 | 501 | 511 | PF00134 | 0.339 |
DOC_CYCLIN_RxL_1 | 569 | 581 | PF00134 | 0.452 |
DOC_CYCLIN_RxL_1 | 616 | 627 | PF00134 | 0.436 |
DOC_CYCLIN_yCln2_LP_2 | 464 | 470 | PF00134 | 0.249 |
DOC_CYCLIN_yCln2_LP_2 | 857 | 863 | PF00134 | 0.499 |
DOC_MAPK_gen_1 | 333 | 341 | PF00069 | 0.361 |
DOC_MAPK_gen_1 | 445 | 452 | PF00069 | 0.246 |
DOC_MAPK_gen_1 | 569 | 577 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 887 | 894 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 190 | 197 | PF00069 | 0.250 |
DOC_MAPK_MEF2A_6 | 887 | 894 | PF00069 | 0.503 |
DOC_PP1_RVXF_1 | 335 | 342 | PF00149 | 0.232 |
DOC_PP1_RVXF_1 | 421 | 427 | PF00149 | 0.232 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.232 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 781 | 785 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 808 | 812 | PF00917 | 0.501 |
DOC_USP7_MATH_2 | 829 | 835 | PF00917 | 0.537 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.232 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 151 | 158 | PF00244 | 0.232 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.223 |
LIG_14-3-3_CanoR_1 | 213 | 223 | PF00244 | 0.220 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.291 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 7 | 15 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 809 | 813 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 859 | 864 | PF00244 | 0.460 |
LIG_APCC_ABBA_1 | 139 | 144 | PF00400 | 0.232 |
LIG_BIR_III_4 | 328 | 332 | PF00653 | 0.400 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.236 |
LIG_BRCT_BRCA1_1 | 382 | 386 | PF00533 | 0.238 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.393 |
LIG_BRCT_BRCA1_2 | 382 | 388 | PF00533 | 0.322 |
LIG_Clathr_ClatBox_1 | 610 | 614 | PF01394 | 0.420 |
LIG_EH1_1 | 201 | 209 | PF00400 | 0.232 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.232 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.232 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.250 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.503 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.612 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.534 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.528 |
LIG_FHA_1 | 894 | 900 | PF00498 | 0.531 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.232 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.280 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.339 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.232 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.625 |
LIG_FHA_2 | 731 | 737 | PF00498 | 0.648 |
LIG_FHA_2 | 860 | 866 | PF00498 | 0.457 |
LIG_FHA_2 | 896 | 902 | PF00498 | 0.588 |
LIG_GBD_Chelix_1 | 204 | 212 | PF00786 | 0.246 |
LIG_GBD_Chelix_1 | 567 | 575 | PF00786 | 0.440 |
LIG_GBD_Chelix_1 | 679 | 687 | PF00786 | 0.449 |
LIG_LIR_Apic_2 | 122 | 128 | PF02991 | 0.232 |
LIG_LIR_Apic_2 | 391 | 397 | PF02991 | 0.232 |
LIG_LIR_Apic_2 | 819 | 825 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 201 | 210 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 377 | 386 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 459 | 468 | PF02991 | 0.232 |
LIG_LIR_Gen_1 | 834 | 842 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 201 | 205 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 377 | 381 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 543 | 547 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 834 | 838 | PF02991 | 0.505 |
LIG_LRP6_Inhibitor_1 | 582 | 594 | PF00058 | 0.451 |
LIG_MAD2 | 516 | 524 | PF02301 | 0.241 |
LIG_NRP_CendR_1 | 941 | 944 | PF00754 | 0.552 |
LIG_PCNA_TLS_4 | 506 | 513 | PF02747 | 0.241 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.303 |
LIG_PTB_Apo_2 | 329 | 336 | PF02174 | 0.362 |
LIG_PTB_Phospho_1 | 329 | 335 | PF10480 | 0.375 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.246 |
LIG_SH2_GRB2like | 55 | 58 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 436 | 440 | PF00017 | 0.232 |
LIG_SH2_NCK_1 | 485 | 489 | PF00017 | 0.227 |
LIG_SH2_PTP2 | 461 | 464 | PF00017 | 0.220 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.311 |
LIG_SH2_SRC | 55 | 58 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 527 | 531 | PF00017 | 0.233 |
LIG_SH2_STAP1 | 606 | 610 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.232 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.575 |
LIG_SH3_2 | 46 | 51 | PF14604 | 0.537 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.611 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.322 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.573 |
LIG_SH3_3 | 822 | 828 | PF00018 | 0.557 |
LIG_SH3_3 | 845 | 851 | PF00018 | 0.503 |
LIG_SH3_3 | 873 | 879 | PF00018 | 0.507 |
LIG_SUMO_SIM_anti_2 | 256 | 263 | PF11976 | 0.237 |
LIG_SUMO_SIM_anti_2 | 491 | 497 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 182 | 189 | PF11976 | 0.255 |
LIG_SUMO_SIM_par_1 | 256 | 263 | PF11976 | 0.232 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.322 |
LIG_TRAF2_1 | 457 | 460 | PF00917 | 0.232 |
LIG_TRAF2_1 | 599 | 602 | PF00917 | 0.428 |
LIG_TRAF2_1 | 785 | 788 | PF00917 | 0.443 |
LIG_TRAF2_1 | 924 | 927 | PF00917 | 0.444 |
LIG_TYR_ITIM | 269 | 274 | PF00017 | 0.300 |
LIG_UBA3_1 | 652 | 660 | PF00899 | 0.485 |
LIG_UBA3_1 | 863 | 867 | PF00899 | 0.461 |
MOD_CDK_SPxxK_3 | 236 | 243 | PF00069 | 0.232 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.241 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.507 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.503 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.371 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.232 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.264 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.255 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.634 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.232 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.468 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.411 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.480 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.638 |
MOD_CK2_1 | 831 | 837 | PF00069 | 0.530 |
MOD_CK2_1 | 859 | 865 | PF00069 | 0.467 |
MOD_CK2_1 | 895 | 901 | PF00069 | 0.598 |
MOD_Cter_Amidation | 160 | 163 | PF01082 | 0.288 |
MOD_Cter_Amidation | 513 | 516 | PF01082 | 0.322 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.264 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.271 |
MOD_GlcNHglycan | 262 | 267 | PF01048 | 0.260 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.583 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.618 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.625 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.529 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.461 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.587 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.509 |
MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.544 |
MOD_GlcNHglycan | 880 | 883 | PF01048 | 0.595 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.485 |
MOD_GlcNHglycan | 937 | 941 | PF01048 | 0.425 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.246 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.234 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.232 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.536 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.595 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.559 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.760 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.442 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.484 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.481 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.526 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.591 |
MOD_GSK3_1 | 804 | 811 | PF00069 | 0.519 |
MOD_GSK3_1 | 893 | 900 | PF00069 | 0.510 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.269 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.560 |
MOD_N-GLC_1 | 730 | 735 | PF02516 | 0.676 |
MOD_N-GLC_2 | 102 | 104 | PF02516 | 0.232 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.252 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.232 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.232 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.262 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.252 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.261 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.422 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.488 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.454 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.622 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.617 |
MOD_NEK2_1 | 709 | 714 | PF00069 | 0.584 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.334 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.232 |
MOD_PIKK_1 | 754 | 760 | PF00454 | 0.627 |
MOD_PKA_1 | 635 | 641 | PF00069 | 0.450 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.523 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.472 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.232 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.608 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.451 |
MOD_PKA_2 | 752 | 758 | PF00069 | 0.549 |
MOD_PKA_2 | 808 | 814 | PF00069 | 0.497 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.437 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.545 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.243 |
MOD_Plk_2-3 | 831 | 837 | PF00069 | 0.527 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.305 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.298 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.232 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.349 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.322 |
MOD_Plk_4 | 808 | 814 | PF00069 | 0.497 |
MOD_Plk_4 | 859 | 865 | PF00069 | 0.463 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.320 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.232 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.476 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.597 |
MOD_SUMO_for_1 | 215 | 218 | PF00179 | 0.232 |
MOD_SUMO_for_1 | 277 | 280 | PF00179 | 0.347 |
MOD_SUMO_for_1 | 59 | 62 | PF00179 | 0.479 |
MOD_SUMO_for_1 | 924 | 927 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 831 | 841 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 912 | 921 | PF00179 | 0.493 |
TRG_DiLeu_BaEn_2 | 217 | 223 | PF01217 | 0.276 |
TRG_DiLeu_BaEn_4 | 459 | 465 | PF01217 | 0.249 |
TRG_DiLeu_BaLyEn_6 | 160 | 165 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 617 | 622 | PF01217 | 0.417 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.240 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.232 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.242 |
TRG_ER_diArg_1 | 468 | 471 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 568 | 570 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 591 | 594 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 619 | 621 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 634 | 636 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 773 | 776 | PF00400 | 0.541 |
TRG_NES_CRM1_1 | 889 | 901 | PF08389 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 213 | 218 | PF00026 | 0.257 |
TRG_Pf-PMV_PEXEL_1 | 221 | 225 | PF00026 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 337 | 342 | PF00026 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 413 | 418 | PF00026 | 0.238 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.287 |
TRG_Pf-PMV_PEXEL_1 | 608 | 612 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 619 | 624 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 681 | 685 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 888 | 893 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEK8 | Leptomonas seymouri | 76% | 100% |
A0A1X0NSC2 | Trypanosomatidae | 63% | 100% |
A0A3Q8IB80 | Leishmania donovani | 29% | 100% |
A0A3Q8IQX0 | Leishmania donovani | 30% | 100% |
A0A3S7WZX1 | Leishmania donovani | 26% | 100% |
A0A3S7X203 | Leishmania donovani | 25% | 100% |
A4HEU5 | Leishmania braziliensis | 88% | 99% |
A4HEX9 | Leishmania braziliensis | 25% | 100% |
A4HGY1 | Leishmania braziliensis | 29% | 100% |
A4HGY5 | Leishmania braziliensis | 26% | 100% |
A4I219 | Leishmania infantum | 100% | 100% |
A4I253 | Leishmania infantum | 26% | 100% |
A4I412 | Leishmania infantum | 30% | 100% |
A4I417 | Leishmania infantum | 25% | 100% |
C9ZRY8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
E9AY68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9AYA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B099 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B0A4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
Q4Q7Y0 | Leishmania major | 25% | 100% |
Q4Q7Y4 | Leishmania major | 29% | 100% |
Q4Q970 | Leishmania major | 27% | 100% |
Q4Q9A4 | Leishmania major | 96% | 100% |
V5BUG8 | Trypanosoma cruzi | 62% | 100% |