##gff-version 3 Q7Z4L5 UniProtKB Chain 1 1316 . . . ID=PRO_0000291917;Note=Tetratricopeptide repeat protein 21B Q7Z4L5 UniProtKB Repeat 108 141 . . . Note=TPR 1 Q7Z4L5 UniProtKB Repeat 145 178 . . . Note=TPR 2 Q7Z4L5 UniProtKB Repeat 180 211 . . . Note=TPR 3 Q7Z4L5 UniProtKB Repeat 285 323 . . . Note=TPR 4 Q7Z4L5 UniProtKB Repeat 324 357 . . . Note=TPR 5 Q7Z4L5 UniProtKB Repeat 492 525 . . . Note=TPR 6 Q7Z4L5 UniProtKB Repeat 563 596 . . . Note=TPR 7 Q7Z4L5 UniProtKB Repeat 617 650 . . . Note=TPR 8 Q7Z4L5 UniProtKB Repeat 722 755 . . . Note=TPR 9 Q7Z4L5 UniProtKB Repeat 757 789 . . . Note=TPR 10 Q7Z4L5 UniProtKB Repeat 791 822 . . . Note=TPR 11 Q7Z4L5 UniProtKB Repeat 831 864 . . . Note=TPR 12 Q7Z4L5 UniProtKB Repeat 884 917 . . . Note=TPR 13 Q7Z4L5 UniProtKB Repeat 919 951 . . . Note=TPR 14 Q7Z4L5 UniProtKB Repeat 952 985 . . . Note=TPR 15 Q7Z4L5 UniProtKB Repeat 1023 1056 . . . Note=TPR 16 Q7Z4L5 UniProtKB Repeat 1197 1230 . . . Note=TPR 17 Q7Z4L5 UniProtKB Repeat 1232 1264 . . . Note=TPR 18 Q7Z4L5 UniProtKB Repeat 1266 1299 . . . Note=TPR 19 Q7Z4L5 UniProtKB Alternative sequence 463 482 . . . ID=VSP_026306;Note=In isoform 2. PASPGQPLCPLLRRCISVLE->VSNYGTYFQGCVYLMFYERT;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:12880961;Dbxref=PMID:12880961 Q7Z4L5 UniProtKB Alternative sequence 483 1316 . . . ID=VSP_026307;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303|PubMed:12880961;Dbxref=PMID:12880961 Q7Z4L5 UniProtKB Natural variant 60 60 . . . ID=VAR_065514;Note=Found in a patient with Meckel-Gruber like syndrome also carrying variant C-671 in BBS7%3B uncertain significance%3B hypomorphic variant in vitro. F->Y;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs371571631,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 66 66 . . . ID=VAR_065515;Note=K->R;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=PMID:21258341 Q7Z4L5 UniProtKB Natural variant 150 150 . . . ID=VAR_065516;Note=In NPHP12%3B with extra-renal features%3B functionally null mutation in vitro. W->R;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=PMID:21258341 Q7Z4L5 UniProtKB Natural variant 157 157 . . . ID=VAR_065517;Note=Found in a patient with Bardet-Biedl syndrome%3B probably acts as a disease modifier%3B the patient also carries a frameshift mutation and variant M-501 in BBS12%3B hypomorphic variant in vitro. K->E;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=PMID:21258341 Q7Z4L5 UniProtKB Natural variant 201 201 . . . ID=VAR_032888;Note=V->M;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:12880961,ECO:0000269|PubMed:14702039,ECO:0000269|PubMed:15489334;Dbxref=dbSNP:rs1432273,PMID:12880961,PMID:14702039,PMID:15489334 Q7Z4L5 UniProtKB Natural variant 209 209 . . . ID=VAR_065518;Note=In NPHP12%3B also found in a patient with Bardet-Biedl syndrome carrying two variants in BBS4%3B hypomorphic variant in vitro. P->L;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs140511594,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 222 222 . . . ID=VAR_065519;Note=Found in a patient with Meckel-Gruber like syndrome also carrying variant V-280 on the same allele and variant G-1183 in RPGRIP1L%3B uncertain significance%3B hypomorphic variant in vitro. Q->L;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs80026831,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 231 231 . . . ID=VAR_065520;Note=In SRTD4 and NPHP12%3B also found in a patient with Bardet-Biedl syndrome carrying variants L-159 and T-346 in BBS12%3B also found in a patient with Meckel-Gruber syndrome carrying a homozygous variant in TMEM216%3B hypomorphic variant in vitro. T->S;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs149925563,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 242 242 . . . ID=VAR_065521;Note=D->N;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs74447004,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 255 255 . . . ID=VAR_065522;Note=Found in a patient with Bardet-Biedl syndrome%3B probably acts as a disease modifier%3B the patient also carries a frameshift mutation and variant P-34 in BBS10%3B hypomorphic variant in vitro. Y->C;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs377061787,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 276 276 . . . ID=VAR_032889;Note=T->A;Ontology_term=ECO:0000269,ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:12880961,ECO:0000269|PubMed:14702039,ECO:0000269|PubMed:15489334;Dbxref=dbSNP:rs7592429,PMID:12880961,PMID:14702039,PMID:15489334 Q7Z4L5 UniProtKB Natural variant 280 280 . . . ID=VAR_065523;Note=Found in a patient with Meckel-Gruber like syndrome also carrying L-222 on the same allele and variant G-1183 in RPGRIP1L%3B uncertain significance%3B hypomorphic variant in vitro. M->V;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs112868646,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 327 327 . . . ID=VAR_065524;Note=Found in a patient with Meckel-Gruber syndrome also carrying a mutation in CC2D2A%3B uncertain significance%3B hypomorphic variant in vitro. A->S;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=PMID:21258341 Q7Z4L5 UniProtKB Natural variant 347 347 . . . ID=VAR_065525;Note=Found in a patient with Meckel-Gruber syndrome also carrying N-1041 on the same allele%3B uncertain significance%3B hypomorphic variant in vitro. Y->C;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs779121249,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 411 411 . . . ID=VAR_065526;Note=Found in a patient with Bardet-Biedl syndrome%3B probably acts as a disease modifier%3B the patient also carries a homozygous frameshift mutation in BBS7%3B hypomorphic variant in vitro. R->G;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs185089786,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 412 412 . . . ID=VAR_065527;Note=Q->R;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs199873923,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 424 424 . . . ID=VAR_065528;Note=D->E;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs533077805,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 463 463 . . . ID=VAR_032890;Note=P->S;Dbxref=dbSNP:rs16851307 Q7Z4L5 UniProtKB Natural variant 473 473 . . . ID=VAR_032891;Note=L->F;Dbxref=dbSNP:rs2163649 Q7Z4L5 UniProtKB Natural variant 566 566 . . . ID=VAR_065529;Note=In NPHP12%3B uncertain significance%3B functionally null mutation in vitro. H->R;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs146320075,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 591 591 . . . ID=VAR_065530;Note=In JBTS11%3B hypomorphic variant in vitro. S->N;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=PMID:21258341 Q7Z4L5 UniProtKB Natural variant 616 616 . . . ID=VAR_065531;Note=R->C;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs139441507,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 624 624 . . . ID=VAR_065532;Note=I->V;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs77106136,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 645 645 . . . ID=VAR_065533;Note=H->R;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs200291881,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 724 724 . . . ID=VAR_065534;Note=S->T;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs759317777,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 753 753 . . . ID=VAR_065535;Note=Found in a patient with Meckel-Gruber like syndrome carrying variant D-559 in BBS1 and a variant in CC2D2A%3B uncertain significance%3B functionally null mutation in vitro. P->L;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs539769126,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 755 755 . . . ID=VAR_065536;Note=In SRTD4%3B functionally null mutation in vitro. D->Y;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=PMID:21258341 Q7Z4L5 UniProtKB Natural variant 795 795 . . . ID=VAR_065537;Note=In SRTD4%3B functionally null mutation in vitro. L->P;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs387907060,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 844 844 . . . ID=VAR_065538;Note=Found in a patient with Meckel-Gruber syndrome%3B uncertain significance%3B functionally null mutation in vitro. M->V;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs766811699,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 846 846 . . . ID=VAR_032892;Note=K->R;Dbxref=dbSNP:rs7595010 Q7Z4L5 UniProtKB Natural variant 867 867 . . . ID=VAR_065539;Note=In JBTS11%3B functionally null mutation in vitro. R->C;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs746700857,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 867 867 . . . ID=VAR_065540;Note=Found in a patient with Meckel-Gruber syndrome also carrying a homozygous variant in CC2D2A%3B also found in a patient with short-rib thoracic dysplasia without polydactyly compoud heterozygous for causative mutations in IFT81%3B probably acts as a disease modifier%3B functionally null mutation in vitro. R->H;Ontology_term=ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:21258341,ECO:0000269|PubMed:27666822;Dbxref=dbSNP:rs76726265,PMID:21258341,PMID:27666822 Q7Z4L5 UniProtKB Natural variant 869 869 . . . ID=VAR_065541;Note=Found in a patient with Meckel-Gruber like syndrome%3B uncertain significance%3B hypomorphic variant in vitro. Q->R;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs137926033,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 939 939 . . . ID=VAR_065542;Note=Hypomorphic variant in vitro. R->Q;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs751382210,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 939 939 . . . ID=VAR_065543;Note=Functionally null mutation in vitro. R->W;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs151227843,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1002 1002 . . . ID=VAR_065544;Note=Found in a patient with Meckel-Gruber like syndrome%3B uncertain significance%3B also found in patients with Bardet-Bied syndrome%3B uncertain significance%3B also found in a patient with nephronophthisis with extra-renal features%3B uncertain significance%3B hypomorphic variant in vitro. L->V;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs146496725,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1011 1011 . . . ID=VAR_068172;Note=In JBTS11. M->T;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:22425360;Dbxref=dbSNP:rs777427926,PMID:22425360 Q7Z4L5 UniProtKB Natural variant 1011 1011 . . . ID=VAR_065545;Note=M->V;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs761842893,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1035 1035 . . . ID=VAR_065546;Note=Y->C;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs757541819,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1041 1041 . . . ID=VAR_065547;Note=Found in a patient with Meckel-Gruber syndrome also carrying C-347 on the same allele%3B uncertain significance%3B functionally null mutation in vitro. D->N;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1103 1103 . . . ID=VAR_065548;Note=Found in a patient with Bardet-Biedl syndrome%3B probably acts as a disease modifier%3B the patient also carries two mutations in BBS6%3B hypomorphic variant in vitro. T->R;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs1482808126,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1167 1167 . . . ID=VAR_065549;Note=In NPHP12%3B hypomorphic variant in vitro. Y->C;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs1040877016,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1186 1186 . . . ID=VAR_065550;Note=In JBTS11%3B hypomorphic variant in vitro. M->V;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs376308209,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1208 1208 . . . ID=VAR_065551;Note=Found in a patient with Bardet-Biedl syndrome%3B probably acts as a disease modifier%3B the patients also carries two mutations in BBS1%3B functionally null mutation in vitro. I->S;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs189519760,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1284 1284 . . . ID=VAR_065552;Note=D->H;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=dbSNP:rs139537546,PMID:21258341 Q7Z4L5 UniProtKB Natural variant 1311 1311 . . . ID=VAR_065553;Note=R->G;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:21258341;Dbxref=PMID:21258341 Q7Z4L5 UniProtKB Sequence conflict 227 227 . . . Note=D->N;Ontology_term=ECO:0000305;evidence=ECO:0000305 Q7Z4L5 UniProtKB Sequence conflict 669 669 . . . Note=D->G;Ontology_term=ECO:0000305;evidence=ECO:0000305 Q7Z4L5 UniProtKB Sequence conflict 1187 1187 . . . Note=N->D;Ontology_term=ECO:0000305;evidence=ECO:0000305 Q7Z4L5 UniProtKB Helix 3 15 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 19 32 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 37 50 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 53 61 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Turn 62 65 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Turn 67 69 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 70 83 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Beta strand 84 86 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 89 105 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 108 120 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 124 138 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 142 154 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 159 172 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 178 190 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 194 207 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 212 224 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 228 239 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 246 258 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 263 279 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 285 298 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 303 319 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 324 336 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 340 353 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 358 371 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 374 387 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 388 390 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 395 407 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 412 429 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 437 443 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 445 458 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 471 487 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 493 504 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 508 521 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 526 538 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 542 555 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 557 561 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 563 575 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 579 591 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 613 629 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 633 646 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Turn 647 649 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 652 666 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBG Q7Z4L5 UniProtKB Helix 670 678 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 687 700 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 705 718 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 722 734 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 738 749 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 756 768 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 772 784 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 791 801 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 805 814 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 824 843 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 847 871 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 873 875 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 876 896 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 900 913 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 918 930 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 934 947 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 952 964 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 968 981 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 986 999 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1002 1005 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1006 1015 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1019 1021 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1023 1036 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1039 1049 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1055 1068 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1078 1081 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1085 1088 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1091 1110 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1116 1132 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1136 1152 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1157 1169 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1173 1184 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Turn 1190 1192 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1193 1209 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1213 1226 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1231 1243 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1247 1260 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Turn 1261 1263 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1266 1278 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1282 1295 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE Q7Z4L5 UniProtKB Helix 1302 1314 . . . Ontology_term=ECO:0007829;evidence=ECO:0007829|PDB:8BBE