GapMind for catabolism of small carbon sources

 

Alignments for a candidate for fahA in Paraburkholderia phymatum STM815

Align fumarylacetoacetate hydrolase (EC 3.7.1.2) (characterized)
to candidate WP_012399618.1 BPHY_RS00980 FAA hydrolase family protein

Query= reanno::MR1:200835
         (328 letters)



>NCBI__GCF_000020045.1:WP_012399618.1
          Length = 330

 Score =  435 bits (1118), Expect = e-127
 Identities = 212/328 (64%), Positives = 252/328 (76%)

Query: 1   MKLASYNNGRRDGQLMLVSRDLTQTVAVPAIAHTMQQLLDGWELLKPQLQELYDALNEGK 60
           MKLAS  +G RDGQL++VSRDL        IA TMQ++LD W    PQL++LYD LN+G+
Sbjct: 1   MKLASLKDGTRDGQLIVVSRDLHTAAVADTIAPTMQRILDDWTFYAPQLRDLYDELNQGR 60

Query: 61  LPNTQTFDETKCLSPLPRAYQWADGSAYVNHVELVRKARGAEMPETFWTDPLFYQGGSDS 120
             NT +FD  +C++PLPRAYQWADGSAYVNHVELVR+ARGAEMP  FWTDPL YQGGSD 
Sbjct: 61  ARNTFSFDAKECMAPLPRAYQWADGSAYVNHVELVRRARGAEMPPEFWTDPLMYQGGSDD 120

Query: 121 FIAPKADIPLASEDWGIDFESEIAVITDDVPMGVSAENAAKHIKLLMLVNDVSLRNLIPA 180
           FI  K DI  ASE +GIDFE+E+AVIT DVPMG   E A K I+L+ LVNDVSLRNLIPA
Sbjct: 121 FIGAKDDIVCASESFGIDFEAEVAVITGDVPMGAKPEQALKSIRLVTLVNDVSLRNLIPA 180

Query: 181 ELAKGFGFFQSKPSSSFSPVAITPDELGHRWEDSKVHLPLITYLNGELFGRPNAGVDMTF 240
           ELAKGFGFFQSKP++SF+PVA+T DELG  W + +VH P+I + NG+  G+P+AG DM F
Sbjct: 181 ELAKGFGFFQSKPATSFAPVAVTLDELGDAWREGRVHRPMIVHWNGKKVGQPDAGTDMVF 240

Query: 241 NFSQLVSHVAKTRPLGAGAIIGSGTISNYDRSAGSSCLAEKRMLEVIADGKASTPFMRFG 300
           NF QL++H AKTR L AGAI+GSGT+SN D   G  C+AEKR LE I  G A T FMRFG
Sbjct: 241 NFGQLIAHAAKTRHLRAGAIVGSGTVSNKDAKRGYCCIAEKRCLETIESGSAQTEFMRFG 300

Query: 301 DTVRIEMLDDNGVSIFGSIDQKVVEYKA 328
           DTV+IEM D+ G +IFGSIDQ V  ++A
Sbjct: 301 DTVKIEMFDEAGKTIFGSIDQAVAPFEA 328


Lambda     K      H
   0.317    0.134    0.397 

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: 335
Number of extensions: 7
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: 328
Length of database: 330
Length adjustment: 28
Effective length of query: 300
Effective length of database: 302
Effective search space:    90600
Effective search space used:    90600
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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