GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gdhA in Shewanella sp. ANA-3

Align NAD-specific glutamate dehydrogenase; NAD-GDH; NAD(+)-dependent glutamate dehydrogenase; EC 1.4.1.2 (characterized)
to candidate 7024607 Shewana3_1785 glutamate dehydrogenase (NAD) (RefSeq)

Query= SwissProt::Q9HZE0
         (1620 letters)



>FitnessBrowser__ANA3:7024607
          Length = 1614

 Score = 1451 bits (3755), Expect = 0.0
 Identities = 772/1583 (48%), Positives = 1042/1583 (65%), Gaps = 16/1583 (1%)

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+   K  +   +Q  
Sbjct: 90   STHSIIEVIQPDMPFLVDSVGMALNRMGITAHMMLHTPLAIERSAQDVTK--VTYLNQSP 147

Query: 151  DVSQESLMYL-EIDRCAHAGELRALEKAILEVLGEVRVTVADFEPMKAKARELLTWLGKA 209
            D ++   ++L EIDR + + +++ALE+ I  VLG+V  +V D+  M AK  E +  L K 
Sbjct: 148  DSTEHVAVFLIEIDRQSSSVDIKALEREIQSVLGDVAASVNDWSAMSAKLSETIKELPKR 207

Query: 210  KLKVPAEELKEVRSYLEWLLDNHFTFLGYEEFSVADEADGGRMVYDEKSFLGLTRLLRAG 269
                  +EL+E  ++L +L ++HFT LGY ++ +        +V +  S LGL       
Sbjct: 208  PFPGEKQELEEAINFLTYLNNHHFTLLGYRQYDLKRVEGDVELVPNMASSLGLMNKHHKT 267

Query: 270  LSKDDLHIEDYAVAYLREPV---LLSFAKAAHPSRVHRPAYPDYVSIRELDGKGRVIREC 326
              +  L +  ++ +  +E +   LL   K++  SRVHRPAY DY+ I+  D KG V+ E 
Sbjct: 268  QPEQGLLLSSFSDSARKEALDHSLLILTKSSAKSRVHRPAYVDYIGIKRFDKKGNVVGED 327

Query: 327  RFMGLFTSSVYNESVNDIPFIRGKVAEVMRRSGFDTKAHLGKELAQVLEVLPRDDLFQTP 386
            RF+GL+ S+VYN S  +IP +  KV  V+ RSG   ++H  K L  +LE LPRD+L Q  
Sbjct: 328  RFIGLYASNVYNRSPREIPLLNEKVQRVLDRSGLTPRSHDYKALLNILENLPRDELIQAN 387

Query: 387  VDELFSTALAIVRIQERNKIRVFLRKDPYGRFCYCLAYVPRDVYSTETRLKIQQVLMERL 446
            VD+L  TA  ++ +Q+R+K+++F+RKD +GRF  CL YV +D Y+T+ R   Q++L +  
Sbjct: 388  VDDLAHTAHGVLEMQDRDKLKLFVRKDGFGRFLSCLVYVSKDRYNTKLRQDTQRILAQHF 447

Query: 447  QAS-DCEFWTFFSESVLARVQFILRVDPKSRIDIDPARLEEEVIQACRSWQDDYSSLVVE 505
             +  D EF T+FSES LAR  +I++VD  + +D+D A +E  +I+A RSW+D  ++ +  
Sbjct: 448  NSKEDVEFTTYFSESTLARTHYIVKVD-NNNMDVDVAAIENNLIEAARSWEDKLNTALNT 506

Query: 506  NLGEAKGTNVLADFPKGFPAGYRERFAPHFAVVDLQHLLSLSEQRPLVMSFYQP--LAQG 563
             LGE  GT+++  +   F   Y+E   P  AVVD+Q L +L ++  L M FYQP   A  
Sbjct: 507  ALGEEAGTHLMKRYANAFEQSYKEDVLPSSAVVDMQQLEALDDEHKLGMLFYQPQEAALN 566

Query: 564  EQQLHCKLYHADTPLALSDVLPILENLGLRVLGEFPYRLRHQNGREYWIHDFAFTYAEGL 623
            + ++  KL+H D P+ LSDVLP+LEN GLRV+ E PY +   +G  +WI DF  T     
Sbjct: 567  DNKVRLKLFHKDEPIHLSDVLPMLENFGLRVINERPYEVTTSDGSTFWILDFLMTVKVTN 626

Query: 624  DVDIQQLNEILQDAFVHIVSGDAENDAFNRLVLTANLPWRDVALLRAYARYLKQIRLGFD 683
              +I    +  Q A   +     E+D FNR++L + L  R+V++LRAYA+Y++QI   F 
Sbjct: 627  TDNIADSQDRFQTALSQVWQKKLEDDGFNRIILASGLTGREVSVLRAYAKYMRQIDATFS 686

Query: 684  LGYIASALNAHTDIARELVRLFKTRFYLARKLTAEDLEDKQQKLEQAILGALDEVQVLNE 743
              YI      +  IA  LV++F  +F    KL    L     K  + I   LDEV  L++
Sbjct: 687  QAYIEETFGRYPQIADLLVKMFIRKFN--PKLKTRTLG----KFMEQINLRLDEVSSLDD 740

Query: 744  DRILRRYLDLIKATLRTNFYQPDGNGQNKSYFSFKFNPKAIPELPRPVPKYEIFVYSPRV 803
            DRI+RRYLDLI ATLRTNFYQ D  G++KSY SFKF P  IPE+PRP+PK+EIFVYSPRV
Sbjct: 741  DRIIRRYLDLINATLRTNFYQLDAKGESKSYISFKFMPSLIPEMPRPLPKFEIFVYSPRV 800

Query: 804  EGVHLRGGKVARGGLRWSDREEDFRTEVLGLVKAQQVKNAVIVPVGAKGGFVPRRLPLGG 863
            EGVHLR GKVARGGLRWSDR EDFRTEVLGLVKAQQVKN VIVPVGAKGGFV ++LP  G
Sbjct: 801  EGVHLRYGKVARGGLRWSDRREDFRTEVLGLVKAQQVKNTVIVPVGAKGGFVCKQLPTEG 860

Query: 864  SRDEIQAEAIACYRIFISGLLDITDNLKEGEVVPPANVVRHDEDDPYLVVAADKGTATFS 923
             R+    E   CYRIFI  LLDITDN+  GE+V P +VVRHDEDDPYLVVAADKGTATFS
Sbjct: 861  GREAFFTEGQECYRIFIRALLDITDNIVNGEIVHPVDVVRHDEDDPYLVVAADKGTATFS 920

Query: 924  DIANGIAAEYGFWLGDAFASGGSAGYDHKGMGITAKGAWVSVQRHFRERGIDVQKDNISV 983
            DIAN I+ EY FWLGDAFASGGS GYDHK MGITA+G W SV+RHFRE GID Q  + S 
Sbjct: 921  DIANAISQEYNFWLGDAFASGGSNGYDHKKMGITARGGWESVKRHFREVGIDCQTTDFSC 980

Query: 984  IGIGDMAGDVFGNGLLMSDKLQLVAAFNHMHIFIDPNPDAASSFVERQRLFNLPRSSWAD 1043
            +GIGDMAGDVFGNG+L+S   +LVAAFNHMHIF+DPNPD A+S+ ER RLF LPRS+W D
Sbjct: 981  LGIGDMAGDVFGNGMLLSKHTKLVAAFNHMHIFVDPNPDTAASYEERARLFALPRSTWED 1040

Query: 1044 YDAKLISAGGGIFLRSAKSIAITPEMKARFDIQADRLAPTELIHALLKAPVDLLWNGGIG 1103
            Y++KLIS GGGIFLRS+KSI ++ EMK   + +   + PTEL+  LLK PVDL+WNGGIG
Sbjct: 1041 YNSKLISKGGGIFLRSSKSIPLSAEMKQMLETEKTSMTPTELMKELLKMPVDLIWNGGIG 1100

Query: 1104 TYVKSSKETHADVGDKANDGLRVDGRELRAKVVGEGGNLGMTQLARVEFGLHGGANNTDF 1163
            TYVKSS+ETHA+VGD+AND LRV+GRELRAK+VGEGGNLG TQL R+E+  +GG  NTDF
Sbjct: 1101 TYVKSSRETHAEVGDRANDALRVNGRELRAKIVGEGGNLGCTQLGRIEYAANGGRINTDF 1160

Query: 1164 IDNAGGVDCSDHEVNIKILLNEVVQAGDMTEKQRNALLVKMTDAVGALVLGNNYKQTQAL 1223
            +DN GGVDCSD+EVNIKILLN +V  G++T KQRN LL +MT+ VG +VL +   QT+ +
Sbjct: 1161 VDNVGGVDCSDNEVNIKILLNALVAEGELTLKQRNRLLEEMTEEVGQIVLQDCKDQTRTI 1220

Query: 1224 SLAQRRARERIAEYKRLMGDLEARGKLDRALEFLPSDEELAERISAGQGLTRAELSVLIS 1283
            S+ Q R  E++ E  R +  LE  GKLDRALEFLPS+EELAER++ G+ LTR ELSVL++
Sbjct: 1221 SVTQVRGAEQLKEQIRFIQYLEKEGKLDRALEFLPSEEELAERLANGRALTRPELSVLVA 1280

Query: 1284 YSKIDLKESLLKSLVPDDDYLTRDMETAFPALLAEKFGDAMRRHRLKREIVSTQIANDLV 1343
            Y+K+ LKE LL   + +D  L++ +   FP  L E +   M  H L+ EI++T +AN+LV
Sbjct: 1281 YAKMVLKEQLLTQEITEDTLLSQLLIAYFPKQLQELYSHRMVTHPLRGEIIATSLANELV 1340

Query: 1344 NHMGITFVQRLKESTGMSAANVAGAYVIVRDVFHLPHWFRQIENLDYQVPADIQLTLMDE 1403
            N MG+ FVQR+++ TG S A+ A  Y + R+VF L    + I +L+  VPA +Q  ++ +
Sbjct: 1341 NDMGLNFVQRMQDETGASVADAAICYTMAREVFGLAELTKAITDLNGIVPAVVQGEMLHQ 1400

Query: 1404 LMRLGRRATRWFLRSRRNELDAARDVAHFGPRIAALGLKLNELLEGPTRELWQARYQTYV 1463
            L R  RRA RWFLR R       + VA F P    +   ++  L        QA     +
Sbjct: 1401 LRRNMRRACRWFLRHRNRTWSIEQTVAFFKPVFEQIKANVHSYLVEEEAAGIQAEINALI 1460

Query: 1464 DAGVPELLARMVAGTSHLYTLLPIIEASDVTGQDTAEVAKAYFAVGSALDLTWYLQQITN 1523
               VP+ +A +VA  S L++ L I + +    +    VA+ YF +G+ ++L W+L+QI+ 
Sbjct: 1461 KENVPQEVATVVANMSTLFSALDIAQIAQAEEKTVELVAETYFKLGARVELHWFLEQISA 1520

Query: 1524 LPVENNWQALAREAFRDDLDWQQRAITVSVLQMQDGPKEVEARVGLWLEQHLPLVERWRA 1583
             PV N+WQALAR AFR++LDWQQRA+T  VL+      + ++ +  W++ +  L+ERW  
Sbjct: 1521 QPVANHWQALARAAFREELDWQQRALTSVVLRTCSETCDAQSVISQWIDTNQALLERWFH 1580

Query: 1584 MLVELRAASGTDYAMYAVANREL 1606
            ML + + +   ++A ++VA REL
Sbjct: 1581 MLADFKTSQSHEFAKFSVALREL 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: 5604
Number of extensions: 242
Number of successful extensions: 9
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