GapMind for catabolism of small carbon sources

 

Alignments for a candidate for garK in Bacteroides thetaiotaomicron VPI-5482

Align glycerate 2-kinase (EC 2.7.1.165) (characterized)
to candidate 350965 BT1437 conserved hypothetical protein (NCBI ptt file)

Query= BRENDA::P23524
         (381 letters)



>FitnessBrowser__Btheta:350965
          Length = 377

 Score =  315 bits (808), Expect = 1e-90
 Identities = 163/370 (44%), Positives = 235/370 (63%), Gaps = 3/370 (0%)

Query: 2   KIVIAPDSYKESLSASEVAQAIEKGFREIFPDAQYVSVPVADGGEGTVEAMIAATQGAER 61
           K+V+A D +K  LS+SEV +A+E+G + + PD + +  P+ADGGEG +  ++ AT+G  +
Sbjct: 3   KVVVAMDFFKGCLSSSEVEKAVEEGIKLVCPDCEVIRFPIADGGEGILTVLVEATRGTYQ 62

Query: 62  HAWVTGPLGEKVNASWGISGDGKTAFIEMAAASGLELVPAEKRDPLVTTSRGTGELILQA 121
                 PL   +  ++G+SGD + AFIEMA  +GL L+   +R+P++TT+ GTGELIL A
Sbjct: 63  KIIANDPLMRPIETTYGVSGDKRVAFIEMATVNGLPLLSETERNPMLTTTYGTGELILHA 122

Query: 122 LESGATNIIIGIGGSATNDGGAGMVQALGAKLCDANGNEIGFGGGSLNTLNDIDISGLDP 181
           +E G    +IGIGGSATND G GM+QALGA+  + +G  +G GG  L+ +  ID S + P
Sbjct: 123 IEQGYREFVIGIGGSATNDAGVGMLQALGARFLNKDGAVLGEGGEILHRIAAIDFSSVHP 182

Query: 182 RLKDCVIRVACDVTNPLVGDNGASRIFGPQKGASEAMIVELDNNLSHYAEVIKKALHVDV 241
            L+D    +ACDV NP  G  GA+ +F  QKGA +AMI +LD  +  ++ +I      ++
Sbjct: 183 ALEDTRFTIACDVRNPFCGPEGAAHVFARQKGADDAMIEKLDAGMQSFSRLIHSTTGREI 242

Query: 242 KDVPGAGAAGGMGAALMAFLGAELKSGIEIVTTALNLEEHIHDCTLVITGEGRIDSQSIH 301
             VPGAGAAGG+G A +AFL AELK GI+++   L   E I    L+ITGEGR D QS+ 
Sbjct: 243 THVPGAGAAGGLGGAFLAFLNAELKPGIDLLLQTLKFSEKIKGADLIITGEGRTDRQSLM 302

Query: 302 GKVPIGVANVAKKYHKPVIGIAGSLTDDVGVVHQHGIDAVFSVLTSIGTLDEAFRG--AY 359
           GKVP G+   AK+   PVI +AGS+ +D  +++Q G   +FS++ S  +L+ A +   A 
Sbjct: 303 GKVPSGILEEAKRQGIPVIVVAGSI-EDTEILNQAGFQGLFSIIPSPMSLETAMKPEVAK 361

Query: 360 DNICRASRNI 369
            NICR    I
Sbjct: 362 KNICRTVAQI 371


Lambda     K      H
   0.315    0.135    0.385 

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: 385
Number of extensions: 19
Number of successful extensions: 2
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: 381
Length of database: 377
Length adjustment: 30
Effective length of query: 351
Effective length of database: 347
Effective search space:   121797
Effective search space used:   121797
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: 42 (22.0 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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