GapMind for catabolism of small carbon sources

 

Alignments for a candidate for paaJ1 in Azoarcus sp. BH72

Align 3-oxoadipyl-CoA thiolase; EC 2.3.1.174 (characterized, see rationale)
to candidate WP_011765903.1 AZO_RS10980 acetyl-CoA C-acyltransferase

Query= uniprot:A0A2Z5MFE9
         (400 letters)



>NCBI__GCF_000061505.1:WP_011765903.1
          Length = 393

 Score =  298 bits (763), Expect = 2e-85
 Identities = 169/398 (42%), Positives = 245/398 (61%), Gaps = 9/398 (2%)

Query: 3   DAYICDAIRTPIGRYGGALKDVRADDLGAVPIKALIQRNPGVDWRAVDDVIYGCANQAGE 62
           +  +  A+R+ +G +GG+LKD+   +LG V +K  I R  GVD + V     G       
Sbjct: 5   EVVVLSAVRSAVGGFGGSLKDMEPAELGGVVVKEAISR-AGVDPKQVTFATVGNCIPTES 63

Query: 63  DNRNVARMSALLAGLPADAPGATINRLCGSGMDAVGTAARAIKAGEAQLMIAGGVESMTR 122
               VAR++ +  G+  ++    +NRLCGS   A+  +A+AI  G+A   + GGVE M+R
Sbjct: 64  RYPYVARVATIQGGMSMESVAFAVNRLCGSAQQAIVNSAQAILLGDADYAVGGGVEVMSR 123

Query: 123 APFVMGKAASAFTRQAEIHDTTIGWRFVNPLMKRQYGVDSMPETAENVAEQFGISRADQD 182
             ++M     A    A + DT      V  ++   +GV  M  TAEN+A ++GISR +QD
Sbjct: 124 GAYLM----PALRNGARMGDTKAIDAMV-AVLTDPFGVGHMGITAENLAAKWGISREEQD 178

Query: 183 AFALASQQKAARAQRDGTLAQEIVGVEIAQKKGDAIRVTLDEHPRETSLESLARLKGVVR 242
           AFAL SQ++AA A  DG    +IV +    +KG  +  T DEHPR T++E+LA++K   +
Sbjct: 179 AFALESQRRAAEAIADGRFKGQIVPITFETRKGPVVFDT-DEHPRATTMEALAKMKPAFK 237

Query: 243 PDGTVTAGNASGVNDGACALLIASQQAAEQYGLRRRARVVGMATAGVEPRIMGIGPAPAT 302
            DG+VTAGNASG+ND A  L++A    A   G +  AR+V  A AGV   +MG GP P++
Sbjct: 238 KDGSVTAGNASGINDAAAFLVLADAAKASAAGHKPMARLVSYAIAGVPNDLMGEGPIPSS 297

Query: 303 QKLLRQLGMTLDQLDVIELNEAFASQGLAVLRMLGLRDDDPRVNPNGGAIALGHPLGASG 362
           +  L++ G+TLD++D+IE NEAFA+Q L V +  GL  D  + NPNGGAIALGHP+GA+G
Sbjct: 298 KLALQRAGLTLDKIDLIESNEAFAAQSLTVAK--GLELDPAKTNPNGGAIALGHPVGATG 355

Query: 363 ARLVTTALHQLERSNGRFALCTMCIGVGQGIALVIERL 400
           A ++T  LH+L+R+ GR+ + TMCIG GQGI  + ER+
Sbjct: 356 AVIITKLLHELQRTGGRYGMATMCIGGGQGITTIWERI 393


Lambda     K      H
   0.319    0.134    0.386 

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: 406
Number of extensions: 18
Number of successful extensions: 5
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: 400
Length of database: 393
Length adjustment: 31
Effective length of query: 369
Effective length of database: 362
Effective search space:   133578
Effective search space used:   133578
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: 50 (23.9 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