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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HGQ9
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 1 |
GO:0006520 | amino acid metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019748 | secondary metabolic process | 2 | 1 |
GO:0019752 | carboxylic acid metabolic process | 5 | 1 |
GO:0043038 | amino acid activation | 4 | 1 |
GO:0043041 | amino acid activation for nonribosomal peptide biosynthetic process | 5 | 1 |
GO:0043436 | oxoacid metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044550 | secondary metabolite biosynthetic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0019842 | vitamin binding | 3 | 1 |
GO:0031177 | phosphopantetheine binding | 3 | 1 |
GO:0033218 | amide binding | 2 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0072341 | modified amino acid binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 54 | 58 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 555 | 559 | PF00656 | 0.399 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 960 | 962 | PF00675 | 0.626 |
CLV_PCSK_FUR_1 | 490 | 494 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 944 | 946 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 986 | 988 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 944 | 946 | PF00082 | 0.824 |
CLV_PCSK_PC1ET2_1 | 986 | 988 | PF00082 | 0.624 |
CLV_PCSK_PC7_1 | 154 | 160 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 841 | 845 | PF00082 | 0.511 |
CLV_Separin_Metazoa | 551 | 555 | PF03568 | 0.372 |
DEG_APCC_DBOX_1 | 502 | 510 | PF00400 | 0.525 |
DEG_Kelch_Keap1_1 | 460 | 465 | PF01344 | 0.249 |
DEG_SPOP_SBC_1 | 84 | 88 | PF00917 | 0.374 |
DOC_CKS1_1 | 278 | 283 | PF01111 | 0.430 |
DOC_CKS1_1 | 311 | 316 | PF01111 | 0.376 |
DOC_CKS1_1 | 591 | 596 | PF01111 | 0.691 |
DOC_CKS1_1 | 897 | 902 | PF01111 | 0.430 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 231 | 240 | PF00134 | 0.431 |
DOC_CYCLIN_yCln2_LP_2 | 426 | 432 | PF00134 | 0.249 |
DOC_CYCLIN_yCln2_LP_2 | 690 | 696 | PF00134 | 0.540 |
DOC_MAPK_gen_1 | 25 | 33 | PF00069 | 0.394 |
DOC_MAPK_gen_1 | 490 | 499 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 597 | 605 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 786 | 796 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 860 | 870 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 144 | 152 | PF00069 | 0.500 |
DOC_MAPK_MEF2A_6 | 667 | 676 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 789 | 798 | PF00069 | 0.501 |
DOC_PP1_RVXF_1 | 578 | 585 | PF00149 | 0.494 |
DOC_PP2B_LxvP_1 | 570 | 573 | PF13499 | 0.420 |
DOC_PP2B_LxvP_1 | 645 | 648 | PF13499 | 0.550 |
DOC_PP2B_LxvP_1 | 690 | 693 | PF13499 | 0.627 |
DOC_PP4_FxxP_1 | 266 | 269 | PF00568 | 0.430 |
DOC_PP4_FxxP_1 | 575 | 578 | PF00568 | 0.482 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 797 | 801 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 871 | 875 | PF00917 | 0.430 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.171 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 532 | 537 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 739 | 744 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 789 | 794 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 825 | 830 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 896 | 901 | PF00397 | 0.430 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 398 | 403 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 635 | 641 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 789 | 793 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 823 | 829 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 863 | 868 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 919 | 927 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 961 | 966 | PF00244 | 0.633 |
LIG_APCC_ABBA_1 | 437 | 442 | PF00400 | 0.397 |
LIG_APCC_ABBAyCdc20_2 | 162 | 168 | PF00400 | 0.249 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.711 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.378 |
LIG_BRCT_BRCA1_1 | 405 | 409 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 453 | 457 | PF00533 | 0.457 |
LIG_deltaCOP1_diTrp_1 | 894 | 903 | PF00928 | 0.376 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.501 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.376 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.376 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.574 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.598 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.613 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.547 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.349 |
LIG_FHA_1 | 808 | 814 | PF00498 | 0.500 |
LIG_FHA_1 | 908 | 914 | PF00498 | 0.457 |
LIG_FHA_1 | 927 | 933 | PF00498 | 0.486 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.683 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.501 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.501 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.501 |
LIG_FHA_2 | 749 | 755 | PF00498 | 0.530 |
LIG_FHA_2 | 968 | 974 | PF00498 | 0.540 |
LIG_GBD_Chelix_1 | 170 | 178 | PF00786 | 0.249 |
LIG_Integrin_isoDGR_2 | 295 | 297 | PF01839 | 0.249 |
LIG_Integrin_RGD_1 | 26 | 28 | PF01839 | 0.494 |
LIG_LIR_Apic_2 | 263 | 269 | PF02991 | 0.430 |
LIG_LIR_Apic_2 | 574 | 578 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 122 | 132 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 139 | 148 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 370 | 380 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 639 | 649 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 953 | 960 | PF02991 | 0.657 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 139 | 143 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 433 | 437 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 631 | 637 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 754 | 760 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 953 | 959 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 964 | 968 | PF02991 | 0.622 |
LIG_MLH1_MIPbox_1 | 263 | 267 | PF16413 | 0.430 |
LIG_MYND_1 | 734 | 738 | PF01753 | 0.522 |
LIG_NRBOX | 563 | 569 | PF00104 | 0.576 |
LIG_NRBOX | 845 | 851 | PF00104 | 0.505 |
LIG_Pex3_1 | 564 | 575 | PF04882 | 0.577 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.422 |
LIG_SH2_CRK | 634 | 638 | PF00017 | 0.500 |
LIG_SH2_SRC | 459 | 462 | PF00017 | 0.249 |
LIG_SH2_SRC | 655 | 658 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.422 |
LIG_SH2_STAT3 | 440 | 443 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 655 | 658 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 673 | 676 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 708 | 711 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 965 | 968 | PF00017 | 0.650 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.515 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.249 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.376 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.643 |
LIG_SH3_3 | 690 | 696 | PF00018 | 0.502 |
LIG_SH3_3 | 732 | 738 | PF00018 | 0.666 |
LIG_SH3_3 | 930 | 936 | PF00018 | 0.531 |
LIG_SUMO_SIM_anti_2 | 248 | 254 | PF11976 | 0.249 |
LIG_TRAF2_1 | 505 | 508 | PF00917 | 0.516 |
LIG_TRAF2_1 | 563 | 566 | PF00917 | 0.507 |
LIG_TYR_ITIM | 966 | 971 | PF00017 | 0.518 |
LIG_TYR_ITSM | 368 | 375 | PF00017 | 0.430 |
LIG_UBA3_1 | 19 | 25 | PF00899 | 0.331 |
LIG_UBA3_1 | 240 | 247 | PF00899 | 0.249 |
LIG_WRC_WIRS_1 | 326 | 331 | PF05994 | 0.249 |
LIG_WRC_WIRS_1 | 572 | 577 | PF05994 | 0.567 |
MOD_CDK_SPxxK_3 | 331 | 338 | PF00069 | 0.311 |
MOD_CDK_SPxxK_3 | 590 | 597 | PF00069 | 0.679 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.501 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.376 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.482 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.390 |
MOD_CK1_1 | 800 | 806 | PF00069 | 0.430 |
MOD_CK1_1 | 839 | 845 | PF00069 | 0.319 |
MOD_CK1_1 | 923 | 929 | PF00069 | 0.675 |
MOD_CK1_1 | 938 | 944 | PF00069 | 0.521 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.492 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.385 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.440 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.303 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.299 |
MOD_CK2_1 | 744 | 750 | PF00069 | 0.633 |
MOD_CK2_1 | 967 | 973 | PF00069 | 0.643 |
MOD_CK2_1 | 992 | 998 | PF00069 | 0.610 |
MOD_Cter_Amidation | 490 | 493 | PF01082 | 0.376 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.496 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.376 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.664 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.502 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.245 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.529 |
MOD_GlcNHglycan | 841 | 844 | PF01048 | 0.508 |
MOD_GlcNHglycan | 873 | 876 | PF01048 | 0.380 |
MOD_GlcNHglycan | 922 | 925 | PF01048 | 0.662 |
MOD_GlcNHglycan | 941 | 944 | PF01048 | 0.751 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.450 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.378 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.408 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.171 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.423 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.341 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.622 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.426 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.555 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.377 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.513 |
MOD_GSK3_1 | 784 | 791 | PF00069 | 0.510 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.320 |
MOD_GSK3_1 | 919 | 926 | PF00069 | 0.613 |
MOD_GSK3_1 | 935 | 942 | PF00069 | 0.706 |
MOD_GSK3_1 | 950 | 957 | PF00069 | 0.661 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.411 |
MOD_N-GLC_1 | 938 | 943 | PF02516 | 0.657 |
MOD_N-GLC_1 | 950 | 955 | PF02516 | 0.707 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.385 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.430 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.410 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.376 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.315 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.430 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.249 |
MOD_NEK2_1 | 666 | 671 | PF00069 | 0.460 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.570 |
MOD_NEK2_2 | 797 | 802 | PF00069 | 0.249 |
MOD_NEK2_2 | 967 | 972 | PF00069 | 0.492 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.430 |
MOD_PIKK_1 | 344 | 350 | PF00454 | 0.423 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.503 |
MOD_PIKK_1 | 598 | 604 | PF00454 | 0.632 |
MOD_PKA_1 | 961 | 967 | PF00069 | 0.635 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.283 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.469 |
MOD_PKA_2 | 788 | 794 | PF00069 | 0.611 |
MOD_PKA_2 | 822 | 828 | PF00069 | 0.404 |
MOD_PKA_2 | 954 | 960 | PF00069 | 0.677 |
MOD_PKB_1 | 396 | 404 | PF00069 | 0.249 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.444 |
MOD_Plk_1 | 367 | 373 | PF00069 | 0.376 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.445 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.501 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.444 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.376 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.529 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.548 |
MOD_Plk_4 | 841 | 847 | PF00069 | 0.475 |
MOD_Plk_4 | 863 | 869 | PF00069 | 0.402 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.516 |
MOD_Plk_4 | 961 | 967 | PF00069 | 0.714 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.724 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.399 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.171 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.376 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.311 |
MOD_ProDKin_1 | 532 | 538 | PF00069 | 0.642 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.673 |
MOD_ProDKin_1 | 739 | 745 | PF00069 | 0.562 |
MOD_ProDKin_1 | 789 | 795 | PF00069 | 0.413 |
MOD_ProDKin_1 | 825 | 831 | PF00069 | 0.350 |
MOD_ProDKin_1 | 896 | 902 | PF00069 | 0.430 |
MOD_SUMO_rev_2 | 220 | 229 | PF00179 | 0.376 |
MOD_SUMO_rev_2 | 494 | 499 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 723 | 728 | PF00179 | 0.674 |
TRG_DiLeu_BaEn_1 | 878 | 883 | PF01217 | 0.430 |
TRG_DiLeu_BaEn_4 | 565 | 571 | PF01217 | 0.326 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 735 | 740 | PF01217 | 0.666 |
TRG_DiLeu_BaLyEn_6 | 768 | 773 | PF01217 | 0.565 |
TRG_DiLeu_BaLyEn_6 | 845 | 850 | PF01217 | 0.519 |
TRG_DiLeu_LyEn_5 | 878 | 883 | PF01217 | 0.501 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 673 | 676 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 968 | 971 | PF00928 | 0.531 |
TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 396 | 399 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 489 | 492 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 578 | 580 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 945 | 948 | PF00400 | 0.749 |
TRG_NES_CRM1_1 | 168 | 182 | PF08389 | 0.249 |
TRG_NES_CRM1_1 | 807 | 819 | PF08389 | 0.430 |
TRG_NLS_Bipartite_1 | 944 | 965 | PF00514 | 0.696 |
TRG_NLS_MonoExtN_4 | 958 | 965 | PF00514 | 0.654 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 848 | 853 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 860 | 864 | PF00026 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5E5 | Leptomonas seymouri | 52% | 98% |
A0A0S4JM65 | Bodo saltans | 31% | 84% |
A0A3Q8IEY8 | Leishmania donovani | 80% | 100% |
A4I3T3 | Leishmania infantum | 80% | 100% |
E9B025 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q861 | Leishmania major | 79% | 100% |