GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prdF in Flavobacterium sp. LM5

Align proline racemase (EC 5.1.1.4) (characterized)
to candidate WP_024981630.1 BXU11_RS07855 4-hydroxyproline epimerase

Query= BRENDA::A8DEZ8
         (335 letters)



>NCBI__GCF_002017945.1:WP_024981630.1
          Length = 336

 Score =  259 bits (662), Expect = 7e-74
 Identities = 132/326 (40%), Positives = 203/326 (62%), Gaps = 4/326 (1%)

Query: 10  IDSHTAGEATRIVVGGIPNIKGNSMPEKKEYLEENLDYLRTAIMLEPRGHNDMFGSVMTQ 69
           +D+HT G   R+V GG PN+ GN+M EK+++  +  D++R  +M EPRGH+ M GS++  
Sbjct: 9   VDAHTCGNPVRVVAGGGPNLVGNNMSEKRQHFLKEYDWIRKGLMFEPRGHDMMSGSILYP 68

Query: 70  PCCPDADFGIIFMDGGGYLNMCGHGTIGAMTAAIETGVVPAVEPVTHVVMEAPAGIIRGD 129
           P  P+ DFGI+F++  G L MCGHGTIG +T AIE G++   + +  + MEAPAG+++  
Sbjct: 69  PSDPENDFGILFIETSGCLPMCGHGTIGTITIAIEEGLIQP-KVLGKIRMEAPAGLVQIA 127

Query: 130 VTVVDGKAKEVSFLNVPAFLYKEGVEVDLPGVGTVKFDISFGGSFFAIIHASQLGLKIEP 189
                 K   V   NV ++L  EG+ V+ P +G + FD+++GG+++AI+        I+ 
Sbjct: 128 YQQTGKKVDWVRLTNVKSYLAAEGLTVECPELGEITFDVAYGGNYYAIVDPQTNFSGIQN 187

Query: 190 QNAGKLTELAMKLRDIINEKIE--IQHPTLAHIKTVDLVEIYDEPTHPEATYKNVVIFGQ 247
             A K+ + + ++R  IN K      HP  + I+ V  +    +P  P ++ +N V +G 
Sbjct: 188 FTASKIIQYSQEVRKRINAKYPDMFIHPENSTIRDVSHMLWTGDPLDPASSGRNAVFYGD 247

Query: 248 GQVDRSPCGTGTSAKLATLHAKGELKVGEKFVYESILGTLFKGEIVEETKVADFNAVVPK 307
             +DRSPCGTGTSA+LA LHAKG+LK GE F++ES +G+ F G++ EET + +  A+VP 
Sbjct: 248 KAIDRSPCGTGTSARLAQLHAKGKLKKGEDFIHESFIGSKFIGKVEEETTIGNIKAIVPS 307

Query: 308 ITGSAYITGFNHFVIDE-EDPLKHGF 332
           I G A + G+N  +IDE +DP   GF
Sbjct: 308 IQGWAKVYGYNTIIIDEDDDPYAFGF 333


Lambda     K      H
   0.319    0.139    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: 314
Number of extensions: 14
Number of successful extensions: 3
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: 335
Length of database: 336
Length adjustment: 28
Effective length of query: 307
Effective length of database: 308
Effective search space:    94556
Effective search space used:    94556
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 (21.7 bits)
S2: 49 (23.5 bits)

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

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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