GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdhA in Shewanella oneidensis MR-1

Align NAD-specific glutamate dehydrogenase; NAD-GDH; NAD(+)-dependent glutamate dehydrogenase; EC 1.4.1.2 (characterized)
to candidate 201733 SO2593 conserved hypothetical protein (NCBI ptt file)

Query= SwissProt::Q9HZE0
         (1620 letters)



>FitnessBrowser__MR1:201733
          Length = 1614

 Score = 1450 bits (3753), Expect = 0.0
 Identities = 772/1582 (48%), Positives = 1036/1582 (65%), Gaps = 14/1582 (0%)

Query: 31   QVTLFAEQFFSLISLDELTQRRLSDLVGCTLSAWRLLERFDRDQPEVRVYNPDYEKHGWQ 90
            QV  FA   ++ +S D+L  R  SDL G  LS W  L +  + +  +RV+NP   KHGWQ
Sbjct: 30   QVEQFATCLYAHMSKDDLNARNDSDLYGAVLSLWNALNKTPKGETHLRVFNPSQSKHGWQ 89

Query: 91   STHTAVEVLHPDLPFLVDSVRMELNRRGYSIHTLQTNVLSVRRSAKGELKEILPKGSQGK 150
            STH+ +EV+ PD+PFLVDSV M LNR G + H +    L++ RSA+ E+ ++        
Sbjct: 90   STHSIIEVIQPDMPFLVDSVGMALNRMGITAHVMLHTPLAIERSAQ-EVTKVTYLNQSPD 148

Query: 151  DVSQESLMYLEIDRCAHAGELRALEKAILEVLGEVRVTVADFEPMKAKARELLTWLGKAK 210
                 ++  +EIDR +   +++ALE+ I  VL +V  +V D+  M AK  E +  L K  
Sbjct: 149  STEHVAVFLIEIDRQSSTADIKALEREIQSVLADVAASVNDWGAMSAKLSETIKELPKRP 208

Query: 211  LKVPAEELKEVRSYLEWLLDNHFTFLGYEEFSVADEADGGRMVYDEKSFLGLTRLLRAGL 270
                 +EL+E  ++L +L ++HFT LGY ++ +        +V +  S LGL        
Sbjct: 209  FPGEKQELEEAINFLTYLNNHHFTLLGYRQYDLKRVEGDVELVPNIASSLGLMNKHHKTQ 268

Query: 271  SKDDLHIEDYAVAYLREPV---LLSFAKAAHPSRVHRPAYPDYVSIRELDGKGRVIRECR 327
             +  L +  ++ +  +E +   LL   K++  SRVHRPAY DY+ I+  D KG VI E R
Sbjct: 269  PEQGLLLSSFSDSARKEALDHSLLILTKSSAKSRVHRPAYVDYIGIKRFDKKGNVIGEDR 328

Query: 328  FMGLFTSSVYNESVNDIPFIRGKVAEVMRRSGFDTKAHLGKELAQVLEVLPRDDLFQTPV 387
            F+GL+ S+VYN S  +IP +  KV  V+ RSG   ++H  K L  +LE LPRD+L Q  V
Sbjct: 329  FIGLYASNVYNRSPREIPLLNEKVQRVLDRSGLTPRSHDYKALLNILENLPRDELIQANV 388

Query: 388  DELFSTALAIVRIQERNKIRVFLRKDPYGRFCYCLAYVPRDVYSTETRLKIQQVLMERLQ 447
            D+L  TA  ++ +Q+R+K+++F+RKD +GRF  CL YV +D Y+T+ R   Q++L +   
Sbjct: 389  DDLAHTAHGVLEMQDRDKLKLFVRKDGFGRFLSCLVYVSKDRYNTKLRQDTQRILAQHFN 448

Query: 448  AS-DCEFWTFFSESVLARVQFILRVDPKSRIDIDPARLEEEVIQACRSWQDDYSSLVVEN 506
            +  D EF T+FSES LAR  +I++VD  + +D+D A +E  +I+A RSW+D  ++ +   
Sbjct: 449  SKEDVEFTTYFSESTLARTHYIVKVD-NNNMDVDVAAIENNLIEAARSWEDKLNTALNNA 507

Query: 507  LGEAKGTNVLADFPKGFPAGYRERFAPHFAVVDLQHLLSLSEQRPLVMSFYQP--LAQGE 564
            LGE  GT+++  +   F   Y+E   P  AVVD+Q L +L ++  L M FYQP   A  +
Sbjct: 508  LGEEAGTHLMKRYANAFEQSYKEDVLPSSAVVDMQQLEALDDEHKLGMLFYQPQEAALND 567

Query: 565  QQLHCKLYHADTPLALSDVLPILENLGLRVLGEFPYRLRHQNGREYWIHDFAFTYAEGLD 624
             ++  KL+H D P+ LSDVLP+LEN GLRV+ E PY +   +G  +WI DF  T      
Sbjct: 568  NKVRLKLFHKDEPIHLSDVLPMLENFGLRVINERPYEVTTADGSTFWILDFLMTVKVVNT 627

Query: 625  VDIQQLNEILQDAFVHIVSGDAENDAFNRLVLTANLPWRDVALLRAYARYLKQIRLGFDL 684
             +I    +  Q A   +     E+D FNR++L + L  R+V++LRAYA+Y++QI   F  
Sbjct: 628  DNIADSQDRFQTALSQVWQKKLEDDGFNRIILASGLTGREVSVLRAYAKYMRQIDATFSQ 687

Query: 685  GYIASALNAHTDIARELVRLFKTRFYLARKLTAEDLEDKQQKLEQAILGALDEVQVLNED 744
             YI      +  IA  LV++F  +F    KL    L     K  + I   LDEV  L++D
Sbjct: 688  AYIEETFGRYPQIADLLVKMFIRKFN--PKLKTRTLG----KFMEQINLRLDEVSSLDDD 741

Query: 745  RILRRYLDLIKATLRTNFYQPDGNGQNKSYFSFKFNPKAIPELPRPVPKYEIFVYSPRVE 804
            RI+RRYLDLI ATLRTNFYQ D  G++KSY SFKF P  IPE+PRP+PK+EIFVYSPRVE
Sbjct: 742  RIIRRYLDLINATLRTNFYQLDAKGESKSYISFKFMPSLIPEMPRPLPKFEIFVYSPRVE 801

Query: 805  GVHLRGGKVARGGLRWSDREEDFRTEVLGLVKAQQVKNAVIVPVGAKGGFVPRRLPLGGS 864
            GVHLR GKVARGGLRWSDR EDFRTEVLGLVKAQQVKN VIVPVGAKGGFV ++LP  G 
Sbjct: 802  GVHLRYGKVARGGLRWSDRREDFRTEVLGLVKAQQVKNTVIVPVGAKGGFVCKQLPTEGG 861

Query: 865  RDEIQAEAIACYRIFISGLLDITDNLKEGEVVPPANVVRHDEDDPYLVVAADKGTATFSD 924
            R+    E   CYRIFI  LLDITDN+  GE+V P +VVRHDEDDPYLVVAADKGTATFSD
Sbjct: 862  REAFFTEGQECYRIFIRALLDITDNILNGEIVHPVDVVRHDEDDPYLVVAADKGTATFSD 921

Query: 925  IANGIAAEYGFWLGDAFASGGSAGYDHKGMGITAKGAWVSVQRHFRERGIDVQKDNISVI 984
            IAN I+ EY FWLGDAFASGGS GYDHK MGITAKG W SV+RHFRE GID Q  + + +
Sbjct: 922  IANSISLEYNFWLGDAFASGGSNGYDHKKMGITAKGGWESVKRHFREVGIDCQTTDFTCL 981

Query: 985  GIGDMAGDVFGNGLLMSDKLQLVAAFNHMHIFIDPNPDAASSFVERQRLFNLPRSSWADY 1044
            GIGDMAGDVFGNG+L+S   +LVAAFNHMHIFIDPNPDAA+S+ ER RLF LPRSSW DY
Sbjct: 982  GIGDMAGDVFGNGMLLSKHTKLVAAFNHMHIFIDPNPDAATSYEERARLFALPRSSWEDY 1041

Query: 1045 DAKLISAGGGIFLRSAKSIAITPEMKARFDIQADRLAPTELIHALLKAPVDLLWNGGIGT 1104
            ++KLIS GGG+FLRS+KSI ++ EMK     +   + PTE++  LLK PVDL+WNGGIGT
Sbjct: 1042 NSKLISKGGGVFLRSSKSIPLSAEMKQMLGTEKISMTPTEMMKELLKMPVDLIWNGGIGT 1101

Query: 1105 YVKSSKETHADVGDKANDGLRVDGRELRAKVVGEGGNLGMTQLARVEFGLHGGANNTDFI 1164
            YVKSS+ET+A+VGD+AND LRV+GRELRAK+VGEGGNLG TQL R+E+  +GG  NTDF+
Sbjct: 1102 YVKSSRETNAEVGDRANDALRVNGRELRAKIVGEGGNLGCTQLGRIEYAANGGRINTDFV 1161

Query: 1165 DNAGGVDCSDHEVNIKILLNEVVQAGDMTEKQRNALLVKMTDAVGALVLGNNYKQTQALS 1224
            DN GGVDCSD+EVNIKILLN +V  G++T KQRN LL +MT+ VG +VL +   QT+ +S
Sbjct: 1162 DNVGGVDCSDNEVNIKILLNAMVTEGELTLKQRNRLLGEMTEEVGEIVLQDCKDQTRTIS 1221

Query: 1225 LAQRRARERIAEYKRLMGDLEARGKLDRALEFLPSDEELAERISAGQGLTRAELSVLISY 1284
            + Q R  E++ E  R +  LE  GKLDRALEFLPS+EEL ER++ G+ LTR ELSVL++Y
Sbjct: 1222 VTQVRGAEQLKEQIRFIQYLEKEGKLDRALEFLPSEEELTERLANGRALTRPELSVLVAY 1281

Query: 1285 SKIDLKESLLKSLVPDDDYLTRDMETAFPALLAEKFGDAMRRHRLKREIVSTQIANDLVN 1344
            +K+ LKE LL   + +D  L++ +   FP  L E +   M  H L+ EI++T +AN+LVN
Sbjct: 1282 AKMVLKEQLLTPEITEDTLLSQLLIAYFPKKLQELYSARMVTHPLRGEIIATSLANELVN 1341

Query: 1345 HMGITFVQRLKESTGMSAANVAGAYVIVRDVFHLPHWFRQIENLDYQVPADIQLTLMDEL 1404
             MG+ FVQR+++ TG S A+ A  Y + R+VF L    + I +L+  VPA +Q  ++ +L
Sbjct: 1342 DMGLNFVQRMQDETGASVADAAICYTMAREVFGLAELTKSITDLNGIVPAVVQGEMLHQL 1401

Query: 1405 MRLGRRATRWFLRSRRNELDAARDVAHFGPRIAALGLKLNELLEGPTRELWQARYQTYVD 1464
             R  RRA RWFLR R       + VA F P    L   ++  L        QA     + 
Sbjct: 1402 RRNMRRACRWFLRHRNRSWSIEQTVAFFKPVFEQLKANVHSYLAEEEAAGIQAEINALIK 1461

Query: 1465 AGVPELLARMVAGTSHLYTLLPIIEASDVTGQDTAEVAKAYFAVGSALDLTWYLQQITNL 1524
              VP+ +A  VA  S L++ L I + +    +  A VA+ YF +G+ ++L W+L+QI+  
Sbjct: 1462 ENVPQDVASTVANMSTLFSTLDIAQIAQAEEKTVALVAETYFKLGARVELHWFLEQISAQ 1521

Query: 1525 PVENNWQALAREAFRDDLDWQQRAITVSVLQMQDGPKEVEARVGLWLEQHLPLVERWRAM 1584
            PV N+WQALAR AFR++LDWQQRA+T  VL+        ++ + LW+E +  L+ERW  M
Sbjct: 1522 PVTNHWQALARAAFREELDWQQRALTSVVLRTCSATCNAQSVISLWIETNQALLERWFHM 1581

Query: 1585 LVELRAASGTDYAMYAVANREL 1606
            L + + +   ++A ++VA REL
Sbjct: 1582 LADFKTSQNHEFAKFSVALREL 1603


Lambda     K      H
   0.321    0.137    0.403 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 5605
Number of extensions: 242
Number of successful extensions: 8
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 1620
Length of database: 1614
Length adjustment: 51
Effective length of query: 1569
Effective length of database: 1563
Effective search space:  2452347
Effective search space used:  2452347
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 bits)
S2: 61 (28.1 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory