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: 20 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031248 | protein acetyltransferase complex | 3 | 12 |
GO:0031414 | N-terminal protein acetyltransferase complex | 4 | 12 |
GO:0031417 | NatC complex | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0140535 | intracellular protein-containing complex | 2 | 12 |
GO:1902493 | acetyltransferase complex | 4 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1990234 | transferase complex | 3 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H953
Term | Name | Level | Count |
---|---|---|---|
GO:0006473 | protein acetylation | 6 | 12 |
GO:0006474 | N-terminal protein amino acid acetylation | 5 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0017196 | N-terminal peptidyl-methionine acetylation | 6 | 12 |
GO:0018193 | peptidyl-amino acid modification | 5 | 12 |
GO:0018206 | peptidyl-methionine modification | 6 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0031365 | N-terminal protein amino acid modification | 5 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0043543 | protein acylation | 5 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0051604 | protein maturation | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.404 |
CLV_C14_Caspase3-7 | 579 | 583 | PF00656 | 0.418 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 685 | 687 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 737 | 739 | PF00675 | 0.472 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 547 | 549 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 685 | 687 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 736 | 738 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.344 |
CLV_PCSK_PC1ET2_1 | 547 | 549 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.529 |
DEG_APCC_DBOX_1 | 123 | 131 | PF00400 | 0.462 |
DEG_APCC_DBOX_1 | 139 | 147 | PF00400 | 0.385 |
DEG_APCC_DBOX_1 | 348 | 356 | PF00400 | 0.383 |
DEG_APCC_DBOX_1 | 592 | 600 | PF00400 | 0.390 |
DEG_APCC_DBOX_1 | 639 | 647 | PF00400 | 0.369 |
DEG_APCC_KENBOX_2 | 525 | 529 | PF00400 | 0.398 |
DEG_SCF_TRCP1_1 | 60 | 65 | PF00400 | 0.338 |
DEG_SPOP_SBC_1 | 153 | 157 | PF00917 | 0.494 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.439 |
DOC_ANK_TNKS_1 | 684 | 691 | PF00023 | 0.501 |
DOC_CKS1_1 | 267 | 272 | PF01111 | 0.557 |
DOC_CYCLIN_yCln2_LP_2 | 117 | 123 | PF00134 | 0.360 |
DOC_CYCLIN_yCln2_LP_2 | 166 | 169 | PF00134 | 0.593 |
DOC_CYCLIN_yCln2_LP_2 | 511 | 517 | PF00134 | 0.335 |
DOC_MAPK_gen_1 | 254 | 263 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 547 | 553 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 593 | 599 | PF00069 | 0.532 |
DOC_MAPK_RevD_3 | 421 | 436 | PF00069 | 0.369 |
DOC_PP1_RVXF_1 | 199 | 205 | PF00149 | 0.294 |
DOC_PP1_RVXF_1 | 257 | 264 | PF00149 | 0.394 |
DOC_PP2B_LxvP_1 | 166 | 169 | PF13499 | 0.594 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.485 |
DOC_PP4_MxPP_1 | 4 | 7 | PF00568 | 0.615 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.221 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 629 | 633 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.563 |
DOC_WD40_RPTOR_TOS_1 | 499 | 504 | PF00400 | 0.456 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.416 |
LIG_14-3-3_CanoR_1 | 245 | 249 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 382 | 388 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 401 | 406 | PF00244 | 0.238 |
LIG_14-3-3_CanoR_1 | 409 | 419 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 436 | 442 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 476 | 481 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 577 | 586 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 635 | 643 | PF00244 | 0.521 |
LIG_Actin_WH2_2 | 376 | 393 | PF00022 | 0.488 |
LIG_BRCT_BRCA1_1 | 535 | 539 | PF00533 | 0.445 |
LIG_Clathr_ClatBox_1 | 299 | 303 | PF01394 | 0.474 |
LIG_Clathr_ClatBox_1 | 420 | 424 | PF01394 | 0.323 |
LIG_Clathr_ClatBox_1 | 607 | 611 | PF01394 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 15 | 25 | PF00928 | 0.450 |
LIG_eIF4E_1 | 585 | 591 | PF01652 | 0.443 |
LIG_eIF4E_1 | 69 | 75 | PF01652 | 0.434 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.290 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.449 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.334 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.449 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.487 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.411 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.571 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.438 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.540 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.354 |
LIG_FXI_DFP_1 | 116 | 120 | PF00024 | 0.445 |
LIG_LIR_Gen_1 | 115 | 123 | PF02991 | 0.269 |
LIG_LIR_Gen_1 | 15 | 25 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.559 |
LIG_LIR_Gen_1 | 443 | 452 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 97 | 106 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 15 | 21 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 443 | 447 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.440 |
LIG_NRBOX | 211 | 217 | PF00104 | 0.451 |
LIG_NRBOX | 70 | 76 | PF00104 | 0.379 |
LIG_PDZ_Class_1 | 739 | 744 | PF00595 | 0.610 |
LIG_Pex14_1 | 516 | 520 | PF04695 | 0.328 |
LIG_Pex14_2 | 204 | 208 | PF04695 | 0.416 |
LIG_Pex14_2 | 311 | 315 | PF04695 | 0.371 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.412 |
LIG_SH2_CRK | 286 | 290 | PF00017 | 0.395 |
LIG_SH2_CRK | 359 | 363 | PF00017 | 0.286 |
LIG_SH2_CRK | 364 | 368 | PF00017 | 0.360 |
LIG_SH2_CRK | 622 | 626 | PF00017 | 0.505 |
LIG_SH2_GRB2like | 517 | 520 | PF00017 | 0.346 |
LIG_SH2_NCK_1 | 110 | 114 | PF00017 | 0.263 |
LIG_SH2_PTP2 | 98 | 101 | PF00017 | 0.442 |
LIG_SH2_SRC | 98 | 101 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 452 | 456 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 633 | 637 | PF00017 | 0.410 |
LIG_SH2_STAP1 | 652 | 656 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.213 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 718 | 721 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.347 |
LIG_SH3_2 | 320 | 325 | PF14604 | 0.327 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.414 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.354 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.654 |
LIG_SH3_3 | 719 | 725 | PF00018 | 0.391 |
LIG_SUMO_SIM_anti_2 | 233 | 241 | PF11976 | 0.430 |
LIG_SUMO_SIM_anti_2 | 502 | 507 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 478 | 485 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 595 | 601 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 606 | 611 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 91 | 97 | PF11976 | 0.337 |
LIG_SxIP_EBH_1 | 547 | 557 | PF03271 | 0.433 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.457 |
LIG_TRFH_1 | 164 | 168 | PF08558 | 0.549 |
LIG_TYR_ITIM | 620 | 625 | PF00017 | 0.499 |
LIG_UBA3_1 | 289 | 297 | PF00899 | 0.356 |
LIG_UBA3_1 | 351 | 357 | PF00899 | 0.438 |
LIG_UBA3_1 | 596 | 604 | PF00899 | 0.396 |
LIG_WRC_WIRS_1 | 293 | 298 | PF05994 | 0.458 |
LIG_WRC_WIRS_1 | 496 | 501 | PF05994 | 0.365 |
MOD_CDK_SPxK_1 | 266 | 272 | PF00069 | 0.427 |
MOD_CDK_SPxxK_3 | 390 | 397 | PF00069 | 0.451 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.427 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.405 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.484 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.358 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.445 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.402 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.446 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.412 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.410 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.423 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.440 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.419 |
MOD_CK2_1 | 504 | 510 | PF00069 | 0.329 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.525 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.461 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.428 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.525 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.416 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.448 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.568 |
MOD_GlcNHglycan | 705 | 708 | PF01048 | 0.411 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.514 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.369 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.482 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.381 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.417 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.286 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.402 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.369 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.411 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.495 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.483 |
MOD_LATS_1 | 100 | 106 | PF00433 | 0.443 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.404 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.534 |
MOD_N-GLC_1 | 337 | 342 | PF02516 | 0.500 |
MOD_N-GLC_1 | 527 | 532 | PF02516 | 0.359 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.381 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.497 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.410 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.413 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.459 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.359 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.388 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.482 |
MOD_NEK2_1 | 556 | 561 | PF00069 | 0.339 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.473 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.367 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.422 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.517 |
MOD_PIKK_1 | 504 | 510 | PF00454 | 0.344 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.316 |
MOD_PKA_1 | 219 | 225 | PF00069 | 0.492 |
MOD_PKA_1 | 409 | 415 | PF00069 | 0.241 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.445 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.393 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.407 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.430 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.368 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.350 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.438 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.473 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.532 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.537 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.501 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.346 |
MOD_Plk_1 | 527 | 533 | PF00069 | 0.425 |
MOD_Plk_1 | 581 | 587 | PF00069 | 0.503 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.463 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.495 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.321 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.399 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.528 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.426 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.414 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.390 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.341 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.394 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.442 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.513 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.418 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.473 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.407 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.427 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.415 |
MOD_SUMO_for_1 | 29 | 32 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 246 | 256 | PF00179 | 0.537 |
MOD_SUMO_rev_2 | 50 | 59 | PF00179 | 0.420 |
MOD_SUMO_rev_2 | 587 | 596 | PF00179 | 0.422 |
TRG_DiLeu_BaEn_1 | 162 | 167 | PF01217 | 0.560 |
TRG_DiLeu_BaEn_1 | 233 | 238 | PF01217 | 0.348 |
TRG_DiLeu_BaEn_1 | 592 | 597 | PF01217 | 0.353 |
TRG_DiLeu_BaEn_2 | 394 | 400 | PF01217 | 0.297 |
TRG_DiLeu_BaLyEn_6 | 317 | 322 | PF01217 | 0.324 |
TRG_DiLeu_BaLyEn_6 | 614 | 619 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 622 | 625 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.311 |
TRG_ER_diArg_1 | 349 | 351 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 684 | 686 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 735 | 738 | PF00400 | 0.532 |
TRG_NES_CRM1_1 | 291 | 303 | PF08389 | 0.465 |
TRG_NES_CRM1_1 | 494 | 508 | PF08389 | 0.373 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4Y3 | Leptomonas seymouri | 78% | 100% |
A0A0S4IMZ6 | Bodo saltans | 32% | 100% |
A0A1X0NSS7 | Trypanosomatidae | 51% | 100% |
A0A3R7M3C6 | Trypanosoma rangeli | 48% | 100% |
A0A3S7WUK2 | Leishmania donovani | 91% | 100% |
A4HXH5 | Leishmania infantum | 91% | 100% |
C9ZP62 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AR70 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QE93 | Leishmania major | 90% | 100% |
V5D6H5 | Trypanosoma cruzi | 48% | 100% |