GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pta in Lutibaculum baratangense AMV1

Align phosphotransacetylase (EC 2.3.1.8) (characterized)
to candidate WP_023431506.1 N177_RS06645 NADP-dependent malic enzyme

Query= metacyc::MONOMER-13062
         (328 letters)



>NCBI__GCF_000496075.1:WP_023431506.1
          Length = 760

 Score =  154 bits (389), Expect = 7e-42
 Identities = 99/305 (32%), Positives = 154/305 (50%), Gaps = 3/305 (0%)

Query: 17  KLVFPEGEDERIISAASRLANDDLAIPVLLGNEAEIKKTADALNVSL-DGIEIVDIENVP 75
           ++VF EGE+E++I AA+  +   L  P+L+G   EI++T D + +S  +GIEIV+     
Sbjct: 453 RVVFAEGEEEQVIRAAAAFSQAGLGQPILVGRNEEIERTMDHMGLSAREGIEIVNARVSD 512

Query: 76  GEVRQQMVQAIVERRKGKTTADQAAQWLKDPNYFGTTMVYMDDVDGMVSGAAHPTGDTVR 135
                     +  +R+G    D       D N F  +MV M D D +V+G        VR
Sbjct: 513 RRTAYAERLYVRLQRQGYLLRDCTRLVNTDRNVFAASMVAMGDADALVTGVTRNYAAAVR 572

Query: 136 PALQIIKTKPGVNLISGSFVMQKGDQRYLFADCAININPNETQLAEIAVESGKTARLFDI 195
               +I  KPG  +I  S ++ +G +  L AD AI+  P   ++AEIAVE+   AR    
Sbjct: 573 DVRLVIDEKPGHRVIGVSLIVARG-RTVLVADTAIHEMPEAEEIAEIAVEAAAAARRLGY 631

Query: 196 DPRVALLSFSTNGSAKSPEVEKVHNATKLAQEMDPAMPIDGEMQFDAAFVPAVAKAKYSD 255
            PRVA++++ST G+  S   EK+  A ++          DGEM  D A  P +  A Y  
Sbjct: 632 RPRVAMVAYSTFGNPDSERSEKMREAVRILDRRKVDFEYDGEMGADVALDPDL-MASYPF 690

Query: 256 SKVAGHATVFVFPELQSGNIGYKIAQRMGGFEAIGPILQGLNKPVSDLSRGCNAEDVYKV 315
            +++G A V V P + S +I  K+ + +GG   +GP+L GL++ V     G    D+  +
Sbjct: 691 CRLSGPANVLVMPAIHSASISTKLLKALGGSRVLGPLLVGLDRAVQIAPMGATDSDLVNI 750

Query: 316 SIITA 320
           + I A
Sbjct: 751 ASIAA 755


Lambda     K      H
   0.315    0.133    0.369 

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: 522
Number of extensions: 23
Number of successful extensions: 4
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: 328
Length of database: 760
Length adjustment: 34
Effective length of query: 294
Effective length of database: 726
Effective search space:   213444
Effective search space used:   213444
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 52 (24.6 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