GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galT in Thermomonospora curvata DSM 43183

Align Galactose-1-phosphate uridylyltransferase; Gal-1-P uridylyltransferase; EC 2.7.7.12; UDP-glucose--hexose-1-phosphate uridylyltransferase (uncharacterized)
to candidate WP_083790008.1 TCUR_RS15505 galactose-1-phosphate uridylyltransferase

Query= curated2:P13212
         (354 letters)



>NCBI__GCF_000024385.1:WP_083790008.1
          Length = 426

 Score =  328 bits (841), Expect = 2e-94
 Identities = 180/354 (50%), Positives = 216/354 (61%), Gaps = 15/354 (4%)

Query: 1   MKKTSTRLADGRELVYYDLRDDTVRDAVDRRPLERTVTTSEVRRDPLLGDSAPSRLAPQG 60
           +++T TRLADGREL+Y+D  +   RDAVD RP       SE+R DPLL +        QG
Sbjct: 83  VRRTVTRLADGRELIYFDRCERPGRDAVDTRPAGGPPPVSELRYDPLLEEWVTIAAHRQG 142

Query: 61  RTYHPPADQCPLCPSGRGTAERDPA--YDVVVFENRFPSL--AGDSGRCEVVCFTSDHDA 116
           RT+ P  D CPLCPS  G     PA  Y+VVV ENRFP+       GRCEVVCF+ DH A
Sbjct: 143 RTFLPGEDACPLCPSAPGRPTEIPAADYEVVVLENRFPTFQPGATGGRCEVVCFSPDHHA 202

Query: 117 SFADLSEEQARLVVDAWTDRTSELSHLPSVEQVFCFENRGAEIGVTLGHPHGQIYAYPFT 176
           SFADL  +Q R V++AW DRT+ELS LP VEQVFCFENRG EIGVTL HPHGQIYAYPF 
Sbjct: 203 SFADLPPQQVRTVIEAWADRTAELSALPGVEQVFCFENRGEEIGVTLRHPHGQIYAYPFV 262

Query: 177 TPRTALMLRSLAAHKDATGGGNLFDSVLEEELAGERVVLEGEHWAAFVAYGAHWPYEVHL 236
            PRT  ML ++  H + TGG    + +  E  AG RVV   E W AFV + A WP+EVHL
Sbjct: 263 PPRTRQMLAAVRRHAERTGGDLFAELLAAEREAGTRVVAANELWTAFVPHAARWPFEVHL 322

Query: 237 YPKRRVPDLLGLDEAARTEFPKVYLELLRRFDRIFGEGEPPTPYIAAWHQAPF-GQLEFE 295
           YP RRVPD+  L+EA R  F  +YL++L RFDR+FG    P PY+AAWHQAP   + E  
Sbjct: 323 YPHRRVPDICALEEAERDAFAALYLDVLGRFDRLFGR---PMPYVAAWHQAPVRHERELA 379

Query: 296 GVTRDDFALHLNFSLPPYVRQAEVPRGLRIRHERVHQRDVPPERAAERLREVAD 349
            +    F++        Y+  +E   G  I        DV PE AA  LR   D
Sbjct: 380 YLHLRLFSIRRAADRLKYLAGSESAMGAFI-------NDVRPEEAARLLRAAGD 426


Lambda     K      H
   0.320    0.138    0.425 

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: 564
Number of extensions: 26
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: 354
Length of database: 426
Length adjustment: 30
Effective length of query: 324
Effective length of database: 396
Effective search space:   128304
Effective search space used:   128304
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