GapMind for catabolism of small carbon sources

 

Alignments for a candidate for padB in Thauera aminoaromatica S2

Align Phenylacetyl-CoA:acceptor oxidoreductase large subunit PadB; EC 1.8.5.3 (characterized, see rationale)
to candidate WP_004303018.1 C665_RS06145 molybdopterin oxidoreductase

Query= uniprot:A0A2R4BLL6
         (914 letters)



>NCBI__GCF_000310185.1:WP_004303018.1
          Length = 913

 Score = 1705 bits (4415), Expect = 0.0
 Identities = 808/912 (88%), Positives = 851/912 (93%)

Query: 3   TPNCPTGVTKVATYCYQCVAGPDLLKVKVEDGVATAIEPNFDAEGVHPAAGRVCVKAFGL 62
           T + P G TKVATYCYQCVAGPDLLKVKVEDGVATA+EPNFDAE VHPAAGRVCVKAFGL
Sbjct: 2   TVSSPQGTTKVATYCYQCVAGPDLLKVKVEDGVATAVEPNFDAEDVHPAAGRVCVKAFGL 61

Query: 63  VQKTYNPNRVLTPMKRTNPKKGRDEDPGFVPISWDEALDLIADKLNTVRANGLLDASGYP 122
           VQKTYNPNRVL PMKRTNPKKGR EDP FVPISWDEALD IA KL  +R  GLLDASGYP
Sbjct: 62  VQKTYNPNRVLQPMKRTNPKKGRHEDPRFVPISWDEALDTIAAKLRGIRETGLLDASGYP 121

Query: 123 RVAASFGGGGTPTAYMGTFPAFLSAWGPVDLSFGSGQGVKCTHSEHLYGELWHRAFTVCP 182
           RVAASFGGGGTPTAYMGTFPA L+AWGPVD+SFGSGQGVKC HSEHLYGELWHRAF VCP
Sbjct: 122 RVAASFGGGGTPTAYMGTFPALLAAWGPVDMSFGSGQGVKCYHSEHLYGELWHRAFIVCP 181

Query: 183 DTPRTKYIVSFGSNIEASGGVCGVWRHAEARVEQGVKRVQVEPHLSVTGGCSAEWVPIKP 242
           DTPR+KYI+SFGSNIEASGGVCGVWRHA ARVEQGVKRVQVEPHLSVTGGCSAEW+PIKP
Sbjct: 182 DTPRSKYILSFGSNIEASGGVCGVWRHAAARVEQGVKRVQVEPHLSVTGGCSAEWLPIKP 241

Query: 243 KTDPAFMHAMIHVMLFENARTRLDIDFLKHMTASPYLVAPNGLYLRDPDTRKPLVWDLKR 302
           KTD A MHAMIHVMLFENAR+RLDIDFLKHMTASPYLVAPNG YLRDPDTRKPLVWDLK 
Sbjct: 242 KTDAACMHAMIHVMLFENARSRLDIDFLKHMTASPYLVAPNGFYLRDPDTRKPLVWDLKS 301

Query: 303 AAAVPFDTADIDPALDGEFTASGLEVLPDNETVDHVQVRVLTAFGKLAEHERTFTPEWAA 362
             AV FDT  IDPALDG+F ASGLEVLPD E V H    V +AFGKL +HERTFTPEWA 
Sbjct: 302 GKAVVFDTPGIDPALDGDFLASGLEVLPDQELVTHEAAPVRSAFGKLLDHERTFTPEWAQ 361

Query: 363 KVCDVPADTIRRVANEYLDHAQIGATIEIEGRTLPFRPVAITLGKTVNNGWGGYDCCWAR 422
            +CDVPA TIRR+ANEYLDHA+IGATIEIEGRTLP+RPVA+TLGKTVNNGWGGYDCCWAR
Sbjct: 362 GICDVPAATIRRIANEYLDHAEIGATIEIEGRTLPYRPVAVTLGKTVNNGWGGYDCCWAR 421

Query: 423 TLMACLVGALDVPGGTIGTTVRLNRPASDRQSSAKPGPDGFMDYPFNPTDKENWVSRPQI 482
           TLMACLVGALDVPGGTIGT VRLNRPA+DRQSSAKPG DGFMDYPFNPTDKENW+SRPQI
Sbjct: 422 TLMACLVGALDVPGGTIGTAVRLNRPANDRQSSAKPGVDGFMDYPFNPTDKENWISRPQI 481

Query: 483 RNANRTLVPLVANSAWSAALGPTHLAWMQQRHGFENFPEPTQPDVWFFYRTNPVISFWDT 542
           RNANRTLVPLVANSAWSAALGPTHLAWMQQRHGFE+FPEPTQPDVWFFYRTNPVISFWDT
Sbjct: 482 RNANRTLVPLVANSAWSAALGPTHLAWMQQRHGFESFPEPTQPDVWFFYRTNPVISFWDT 541

Query: 543 PQVAEAVSKFPFVVAFTYTRDETNHFADVLLPDCTDLEGLQLIRIGGTKYVEQFWDKQGF 602
           PQVAEAV+KFPFVVAFTYTRDETNHFAD+LLPDCTDLEGLQ++RIGGTKYVEQFWD QGF
Sbjct: 542 PQVAEAVAKFPFVVAFTYTRDETNHFADILLPDCTDLEGLQMLRIGGTKYVEQFWDHQGF 601

Query: 603 ALRQPAVVPQGETRDFTWIASELARRAGIQEPYNKAINRGAAGVPLKGASYDFSLDLEQT 662
           ALRQP V  QG+TRDFTWI++ELARRAGI EPYNKAINRGAAGVPLKG +YDFSL  +  
Sbjct: 602 ALRQPVVPTQGDTRDFTWISTELARRAGILEPYNKAINRGAAGVPLKGPNYDFSLQPDHA 661

Query: 663 HGVEEIWNASCRAASAELTGGAEDHGLDWWREHGFRTIDYPRLQWYLYPHMKDNGLRFEM 722
           +GVEEIW+ASCRAASAELT GAEDHGL+WW+EHGFRTI YPRLQWYLYPH+ D GLRFEM
Sbjct: 662 YGVEEIWDASCRAASAELTEGAEDHGLEWWKEHGFRTIKYPRLQWYLYPHLVDQGLRFEM 721

Query: 723 PYQERIFRIGTELGRRLHESGIDWWDRQLTEYQPLPDFHDFSHLIKSAVISNLGGREEDF 782
           PYQERI+RIG ELGRRLHESGIDWWDRQLTEY+PLP+FHDFSHLIK AVISNLGGR+EDF
Sbjct: 722 PYQERIYRIGEELGRRLHESGIDWWDRQLTEYRPLPEFHDFSHLIKHAVISNLGGRDEDF 781

Query: 783 PFWLLTSRSMQYAWGGNVSLQMVREVAANVAGHRGVIMNPASAAKLGIEDGDLVEVRSPL 842
           PFWLLT+RSMQY+WGGNVSLQMVREVAANV GHRGVIMNP +A KLGIEDGDLVEVRSPL
Sbjct: 782 PFWLLTARSMQYSWGGNVSLQMVREVAANVKGHRGVIMNPTAARKLGIEDGDLVEVRSPL 841

Query: 843 RETRGRVVLRQGIRPDTLLMVGQFDHWITPYAKDFDVPSMNSLVPMLMDLTDATGSAADI 902
           RETRGRVVLRQGIRPDTLLMVGQFDHWITPYAKDFDVPSMN+LVPMLMDLTDATGSAADI
Sbjct: 842 RETRGRVVLRQGIRPDTLLMVGQFDHWITPYAKDFDVPSMNALVPMLMDLTDATGSAADI 901

Query: 903 VPVSIKRVGGAQ 914
           VPVSIKR+GGAQ
Sbjct: 902 VPVSIKRIGGAQ 913


Lambda     K      H
   0.320    0.137    0.438 

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: 3189
Number of extensions: 113
Number of successful extensions: 1
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: 914
Length of database: 913
Length adjustment: 43
Effective length of query: 871
Effective length of database: 870
Effective search space:   757770
Effective search space used:   757770
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 (21.8 bits)
S2: 56 (26.2 bits)

This GapMind analysis is from Sep 24 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