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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HG86
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006356 | regulation of transcription by RNA polymerase I | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 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:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045943 | positive regulation of transcription by RNA polymerase I | 8 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2000232 | regulation of rRNA processing | 6 | 1 |
GO:2000234 | positive regulation of rRNA processing | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 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 | 607 | 611 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 739 | 743 | PF00656 | 0.629 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.525 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 476 | 478 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 654 | 656 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 476 | 478 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.422 |
CLV_Separin_Metazoa | 651 | 655 | PF03568 | 0.428 |
DEG_APCC_DBOX_1 | 554 | 562 | PF00400 | 0.395 |
DEG_APCC_DBOX_1 | 660 | 668 | PF00400 | 0.514 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.527 |
DEG_SCF_FBW7_1 | 318 | 323 | PF00400 | 0.348 |
DEG_SPOP_SBC_1 | 48 | 52 | PF00917 | 0.370 |
DOC_CKS1_1 | 516 | 521 | PF01111 | 0.352 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.458 |
DOC_MAPK_gen_1 | 224 | 232 | PF00069 | 0.285 |
DOC_MAPK_gen_1 | 249 | 257 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 306 | 312 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 224 | 232 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 249 | 257 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 40 | 48 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 466 | 474 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 84 | 91 | PF00069 | 0.368 |
DOC_PP2B_LxvP_1 | 689 | 692 | PF13499 | 0.520 |
DOC_PP4_FxxP_1 | 173 | 176 | PF00568 | 0.358 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.325 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 781 | 785 | PF00917 | 0.396 |
DOC_USP7_MATH_2 | 107 | 113 | PF00917 | 0.467 |
DOC_USP7_UBL2_3 | 26 | 30 | PF12436 | 0.370 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.336 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 209 | 218 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 346 | 356 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 426 | 432 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 480 | 485 | PF00244 | 0.304 |
LIG_14-3-3_CterR_2 | 793 | 795 | PF00244 | 0.432 |
LIG_Actin_WH2_2 | 649 | 667 | PF00022 | 0.529 |
LIG_APCC_ABBA_1 | 170 | 175 | PF00400 | 0.292 |
LIG_APCC_ABBA_1 | 253 | 258 | PF00400 | 0.428 |
LIG_BIR_III_4 | 712 | 716 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 532 | 536 | PF00533 | 0.330 |
LIG_Clathr_ClatBox_1 | 254 | 258 | PF01394 | 0.457 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.687 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.553 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.342 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.508 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.365 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.436 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.441 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.455 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.392 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.355 |
LIG_FHA_1 | 723 | 729 | PF00498 | 0.619 |
LIG_FHA_1 | 777 | 783 | PF00498 | 0.607 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.504 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.440 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.567 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.392 |
LIG_FHA_2 | 761 | 767 | PF00498 | 0.568 |
LIG_LIR_Apic_2 | 775 | 781 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 178 | 187 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 200 | 210 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 64 | 74 | PF02991 | 0.255 |
LIG_LIR_Gen_1 | 701 | 711 | PF02991 | 0.481 |
LIG_LIR_LC3C_4 | 188 | 192 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 501 | 506 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 554 | 559 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 684 | 689 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 701 | 707 | PF02991 | 0.575 |
LIG_MYND_1 | 221 | 225 | PF01753 | 0.501 |
LIG_PCNA_yPIPBox_3 | 135 | 145 | PF02747 | 0.407 |
LIG_Pex14_2 | 202 | 206 | PF04695 | 0.401 |
LIG_Pex14_2 | 265 | 269 | PF04695 | 0.354 |
LIG_REV1ctd_RIR_1 | 731 | 739 | PF16727 | 0.678 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.562 |
LIG_SH2_CRK | 778 | 782 | PF00017 | 0.480 |
LIG_SH2_PTP2 | 256 | 259 | PF00017 | 0.348 |
LIG_SH2_PTP2 | 45 | 48 | PF00017 | 0.323 |
LIG_SH2_SRC | 256 | 259 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 397 | 401 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 391 | 394 | PF00017 | 0.511 |
LIG_SH2_STAT3 | 545 | 548 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 778 | 781 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 790 | 793 | PF00017 | 0.486 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.413 |
LIG_SH3_3 | 212 | 218 | PF00018 | 0.572 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.330 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.506 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.478 |
LIG_SH3_3 | 572 | 578 | PF00018 | 0.494 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.496 |
LIG_SUMO_SIM_anti_2 | 188 | 194 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 292 | 298 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 334 | 341 | PF11976 | 0.432 |
LIG_TYR_ITIM | 254 | 259 | PF00017 | 0.312 |
LIG_UBA3_1 | 138 | 145 | PF00899 | 0.383 |
LIG_WRC_WIRS_1 | 431 | 436 | PF05994 | 0.505 |
LIG_WRC_WIRS_1 | 730 | 735 | PF05994 | 0.685 |
LIG_WRC_WIRS_1 | 737 | 742 | PF05994 | 0.684 |
LIG_WW_3 | 410 | 414 | PF00397 | 0.485 |
MOD_CDC14_SPxK_1 | 410 | 413 | PF00782 | 0.551 |
MOD_CDC14_SPxK_1 | 463 | 466 | PF00782 | 0.410 |
MOD_CDK_SPxK_1 | 407 | 413 | PF00069 | 0.563 |
MOD_CDK_SPxK_1 | 460 | 466 | PF00069 | 0.410 |
MOD_CDK_SPxxK_3 | 574 | 581 | PF00069 | 0.442 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.501 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.492 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.444 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.372 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.373 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.479 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.451 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.370 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.481 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.447 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.432 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.390 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.701 |
MOD_Cter_Amidation | 247 | 250 | PF01082 | 0.422 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.614 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.587 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.425 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.372 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.399 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.415 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.503 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.496 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.389 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.361 |
MOD_GlcNHglycan | 642 | 645 | PF01048 | 0.454 |
MOD_GlcNHglycan | 711 | 716 | PF01048 | 0.742 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.649 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.641 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.515 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.500 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.456 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.472 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.442 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.289 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.405 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.504 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.381 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.467 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.334 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.355 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.469 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.391 |
MOD_GSK3_1 | 707 | 714 | PF00069 | 0.785 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.444 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.680 |
MOD_GSK3_1 | 755 | 762 | PF00069 | 0.638 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.479 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.429 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.381 |
MOD_N-GLC_1 | 511 | 516 | PF02516 | 0.399 |
MOD_N-GLC_1 | 657 | 662 | PF02516 | 0.487 |
MOD_N-GLC_1 | 707 | 712 | PF02516 | 0.492 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.399 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.532 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.463 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.495 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.529 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.438 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.443 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.393 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.487 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.467 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.414 |
MOD_NEK2_1 | 782 | 787 | PF00069 | 0.448 |
MOD_NEK2_2 | 61 | 66 | PF00069 | 0.529 |
MOD_NEK2_2 | 699 | 704 | PF00069 | 0.476 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.323 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.364 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.447 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.400 |
MOD_PIKK_1 | 496 | 502 | PF00454 | 0.391 |
MOD_PIKK_1 | 517 | 523 | PF00454 | 0.532 |
MOD_PIKK_1 | 565 | 571 | PF00454 | 0.425 |
MOD_PIKK_1 | 6 | 12 | PF00454 | 0.397 |
MOD_PIKK_1 | 740 | 746 | PF00454 | 0.635 |
MOD_PIKK_1 | 760 | 766 | PF00454 | 0.469 |
MOD_PK_1 | 79 | 85 | PF00069 | 0.439 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.504 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.612 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.490 |
MOD_PKB_1 | 655 | 663 | PF00069 | 0.323 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.384 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.498 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.401 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.476 |
MOD_Plk_1 | 629 | 635 | PF00069 | 0.464 |
MOD_Plk_1 | 657 | 663 | PF00069 | 0.483 |
MOD_Plk_2-3 | 736 | 742 | PF00069 | 0.681 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.479 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.377 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.447 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.470 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.454 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.423 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.424 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.356 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.348 |
MOD_Plk_4 | 699 | 705 | PF00069 | 0.635 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.686 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.493 |
MOD_Plk_4 | 782 | 788 | PF00069 | 0.464 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.435 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.372 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.443 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.524 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.562 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.366 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.345 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.481 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.663 |
MOD_SUMO_rev_2 | 546 | 552 | PF00179 | 0.293 |
TRG_AP2beta_CARGO_1 | 200 | 209 | PF09066 | 0.417 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 438 | 443 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 557 | 562 | PF01217 | 0.409 |
TRG_DiLeu_LyEn_5 | 554 | 559 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 704 | 707 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 653 | 655 | PF00400 | 0.536 |
TRG_NLS_MonoExtC_3 | 28 | 34 | PF00514 | 0.370 |
TRG_NLS_MonoExtN_4 | 26 | 33 | PF00514 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 560 | 564 | PF00026 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 767 | 771 | PF00026 | 0.575 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4K6 | Leptomonas seymouri | 67% | 97% |
A0A0S4J855 | Bodo saltans | 34% | 100% |
A0A1X0NYJ9 | Trypanosomatidae | 41% | 99% |
A0A3Q8IGL7 | Leishmania donovani | 84% | 100% |
A0A422P1N8 | Trypanosoma rangeli | 41% | 100% |
A4I3A1 | Leishmania infantum | 84% | 100% |
D0A824 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 95% |
E9AZK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q8M4 | Leishmania major | 84% | 100% |