Chaperone/Protein Folding, Heat shock 70 -like (Fragment)
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4I219
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0006458 | 'de novo' protein folding | 3 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006986 | response to unfolded protein | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010033 | response to organic substance | 3 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034620 | cellular response to unfolded protein | 5 | 1 |
GO:0035966 | response to topologically incorrect protein | 3 | 1 |
GO:0035967 | cellular response to topologically incorrect protein | 4 | 1 |
GO:0042026 | protein refolding | 3 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 1 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
GO:0070887 | cellular response to chemical stimulus | 3 | 1 |
GO:0071310 | cellular response to organic substance | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0044183 | protein folding chaperone | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
GO:0031072 | heat shock protein binding | 3 | 1 |
GO:0051082 | unfolded protein binding | 3 | 1 |
GO:0051787 | misfolded protein binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 688 | 692 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.709 |
CLV_PCSK_FUR_1 | 276 | 280 | PF00082 | 0.416 |
CLV_PCSK_FUR_1 | 85 | 89 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 569 | 571 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 650 | 652 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.649 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 635 | 639 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.509 |
CLV_Separin_Metazoa | 675 | 679 | PF03568 | 0.471 |
DEG_SPOP_SBC_1 | 304 | 308 | PF00917 | 0.710 |
DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.627 |
DOC_CKS1_1 | 237 | 242 | PF01111 | 0.317 |
DOC_CYCLIN_RxL_1 | 333 | 342 | PF00134 | 0.318 |
DOC_CYCLIN_RxL_1 | 410 | 420 | PF00134 | 0.317 |
DOC_CYCLIN_RxL_1 | 501 | 511 | PF00134 | 0.417 |
DOC_CYCLIN_RxL_1 | 569 | 581 | PF00134 | 0.661 |
DOC_CYCLIN_RxL_1 | 616 | 627 | PF00134 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 464 | 470 | PF00134 | 0.347 |
DOC_MAPK_gen_1 | 333 | 341 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 445 | 452 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 569 | 577 | PF00069 | 0.656 |
DOC_MAPK_MEF2A_6 | 190 | 197 | PF00069 | 0.317 |
DOC_PP1_RVXF_1 | 335 | 342 | PF00149 | 0.317 |
DOC_PP1_RVXF_1 | 421 | 427 | PF00149 | 0.317 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.717 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.684 |
LIG_14-3-3_CanoR_1 | 151 | 158 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 213 | 223 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 7 | 15 | PF00244 | 0.691 |
LIG_APCC_ABBA_1 | 139 | 144 | PF00400 | 0.317 |
LIG_BIR_III_4 | 328 | 332 | PF00653 | 0.542 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.317 |
LIG_BRCT_BRCA1_1 | 382 | 386 | PF00533 | 0.298 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_2 | 382 | 388 | PF00533 | 0.417 |
LIG_Clathr_ClatBox_1 | 610 | 614 | PF01394 | 0.495 |
LIG_EH1_1 | 201 | 209 | PF00400 | 0.317 |
LIG_EH1_1 | 254 | 262 | PF00400 | 0.410 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.317 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.317 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.342 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.500 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.626 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.592 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.760 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.317 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.385 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.317 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.317 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.697 |
LIG_FHA_2 | 731 | 737 | PF00498 | 0.720 |
LIG_GBD_Chelix_1 | 204 | 212 | PF00786 | 0.342 |
LIG_GBD_Chelix_1 | 567 | 575 | PF00786 | 0.579 |
LIG_GBD_Chelix_1 | 679 | 687 | PF00786 | 0.538 |
LIG_LIR_Apic_2 | 122 | 128 | PF02991 | 0.317 |
LIG_LIR_Apic_2 | 391 | 397 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 201 | 210 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 377 | 386 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 459 | 468 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 201 | 205 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 377 | 381 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 543 | 547 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.601 |
LIG_LRP6_Inhibitor_1 | 582 | 594 | PF00058 | 0.547 |
LIG_MAD2 | 516 | 524 | PF02301 | 0.458 |
LIG_PCNA_TLS_4 | 506 | 513 | PF02747 | 0.458 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.317 |
LIG_PTB_Apo_2 | 329 | 336 | PF02174 | 0.507 |
LIG_PTB_Phospho_1 | 329 | 335 | PF10480 | 0.519 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 55 | 58 | PF00017 | 0.654 |
LIG_SH2_NCK_1 | 436 | 440 | PF00017 | 0.317 |
LIG_SH2_NCK_1 | 485 | 489 | PF00017 | 0.381 |
LIG_SH2_PTP2 | 461 | 464 | PF00017 | 0.287 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.410 |
LIG_SH2_SRC | 55 | 58 | PF00017 | 0.696 |
LIG_SH2_STAP1 | 527 | 531 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 606 | 610 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.637 |
LIG_SH3_2 | 46 | 51 | PF14604 | 0.624 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.700 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.317 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.636 |
LIG_SUMO_SIM_anti_2 | 256 | 263 | PF11976 | 0.317 |
LIG_SUMO_SIM_anti_2 | 491 | 497 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 182 | 189 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 256 | 263 | PF11976 | 0.317 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.417 |
LIG_TRAF2_1 | 457 | 460 | PF00917 | 0.317 |
LIG_TRAF2_1 | 599 | 602 | PF00917 | 0.496 |
LIG_TYR_ITIM | 269 | 274 | PF00017 | 0.402 |
LIG_UBA3_1 | 652 | 660 | PF00899 | 0.546 |
MOD_CDK_SPxxK_3 | 236 | 243 | PF00069 | 0.317 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.458 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.555 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.578 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.417 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.317 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.381 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.341 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.684 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.317 |
MOD_CK2_1 | 540 | 546 | PF00069 | 0.467 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.483 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.527 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.683 |
MOD_Cter_Amidation | 160 | 163 | PF01082 | 0.316 |
MOD_Cter_Amidation | 513 | 516 | PF01082 | 0.417 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.317 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.317 |
MOD_GlcNHglycan | 262 | 267 | PF01048 | 0.317 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.669 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.692 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.691 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.610 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.560 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.641 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.586 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.317 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.317 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.317 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.629 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.679 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.647 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.707 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.499 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.543 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.557 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.571 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.649 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.381 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.763 |
MOD_N-GLC_1 | 730 | 735 | PF02516 | 0.721 |
MOD_N-GLC_2 | 102 | 104 | PF02516 | 0.317 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.317 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.317 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.317 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.317 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.317 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.287 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.404 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.477 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.582 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.683 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.605 |
MOD_NEK2_1 | 709 | 714 | PF00069 | 0.627 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.317 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.317 |
MOD_PKA_1 | 635 | 641 | PF00069 | 0.499 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.677 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.575 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.317 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.686 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.499 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.528 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.685 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.317 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.317 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.342 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.317 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.374 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.417 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.317 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.317 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.674 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.679 |
MOD_SUMO_for_1 | 215 | 218 | PF00179 | 0.317 |
MOD_SUMO_for_1 | 277 | 280 | PF00179 | 0.550 |
MOD_SUMO_for_1 | 59 | 62 | PF00179 | 0.672 |
TRG_DiLeu_BaEn_2 | 217 | 223 | PF01217 | 0.342 |
TRG_DiLeu_BaEn_4 | 459 | 465 | PF01217 | 0.347 |
TRG_DiLeu_BaLyEn_6 | 160 | 165 | PF01217 | 0.317 |
TRG_DiLeu_BaLyEn_6 | 617 | 622 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.623 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 468 | 471 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 568 | 570 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 591 | 594 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 619 | 621 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 634 | 636 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 74 | 77 | PF00400 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 213 | 218 | PF00026 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 221 | 225 | PF00026 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 337 | 342 | PF00026 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 413 | 418 | PF00026 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.375 |
TRG_Pf-PMV_PEXEL_1 | 608 | 612 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 619 | 624 | PF00026 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 681 | 685 | PF00026 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEK8 | Leptomonas seymouri | 81% | 80% |
A0A1X0NSC2 | Trypanosomatidae | 70% | 84% |
A0A3Q8IB80 | Leishmania donovani | 29% | 100% |
A0A3Q8ICR2 | Leishmania donovani | 100% | 79% |
A0A3Q8IQX0 | Leishmania donovani | 29% | 100% |
A0A3S7WZX1 | Leishmania donovani | 26% | 100% |
A0A3S7X203 | Leishmania donovani | 26% | 100% |
A4HEU5 | Leishmania braziliensis | 89% | 100% |
A4HEX9 | Leishmania braziliensis | 25% | 100% |
A4HGY1 | Leishmania braziliensis | 28% | 100% |
A4HGY5 | Leishmania braziliensis | 26% | 100% |
A4I253 | Leishmania infantum | 26% | 100% |
A4I412 | Leishmania infantum | 29% | 100% |
A4I417 | Leishmania infantum | 26% | 100% |
A4X148 | Salinispora tropica (strain ATCC BAA-916 / DSM 44818 / CNB-440) | 27% | 100% |
A8LWM4 | Salinispora arenicola (strain CNS-205) | 27% | 100% |
B8D758 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain Tuc7) | 28% | 100% |
B8D8V4 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain 5A) | 28% | 100% |
C9ZRY8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 85% |
E9AHH0 | Leishmania infantum | 29% | 100% |
E9AHH1 | Leishmania infantum | 29% | 100% |
E9AY68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9AYA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B099 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B0A4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
O32464 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 28% | 100% |
O65719 | Arabidopsis thaliana | 28% | 100% |
P09189 | Petunia hybrida | 28% | 100% |
P22953 | Arabidopsis thaliana | 27% | 100% |
P27322 | Solanum lycopersicum | 28% | 100% |
Q4Q7Y0 | Leishmania major | 25% | 100% |
Q4Q7Y4 | Leishmania major | 28% | 100% |
Q4Q970 | Leishmania major | 27% | 100% |
Q4Q9A4 | Leishmania major | 96% | 100% |
Q6G1F9 | Bartonella quintana (strain Toulouse) | 29% | 100% |
Q6G554 | Bartonella henselae (strain ATCC 49882 / DSM 28221 / Houston 1) | 29% | 100% |
Q7U6R7 | Parasynechococcus marenigrum (strain WH8102) | 29% | 100% |
Q8K9Y8 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 28% | 100% |
Q9LHA8 | Arabidopsis thaliana | 28% | 100% |
V5BUG8 | Trypanosoma cruzi | 69% | 79% |