GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galT in Saccharomonospora cyanea NA-134

Align Galactose-1-phosphate uridylyltransferase; Gal-1-P uridylyltransferase; EC 2.7.7.12; UDP-glucose--hexose-1-phosphate uridylyltransferase (uncharacterized)
to candidate WP_005459317.1 SACCYDRAFT_RS21270 galactose-1-phosphate uridylyltransferase

Query= curated2:P13212
         (354 letters)



>NCBI__GCF_000244975.1:WP_005459317.1
          Length = 351

 Score =  284 bits (727), Expect = 2e-81
 Identities = 172/352 (48%), Positives = 200/352 (56%), Gaps = 20/352 (5%)

Query: 1   MKKTSTRLADGRELVYYDLRD-DTVRDAVDRRPLERTVTTSEVRRDPLLGDSAPSRLAPQ 59
           M KT  RL+DGR + YYD  +    R AVD R L      SEVRRDPL G+        Q
Sbjct: 1   MNKTVRRLSDGRRITYYDEGERPRPRTAVDTRELPEVTAVSEVRRDPLTGELVVIAAHRQ 60

Query: 60  GRTYHPPADQCPLCPSGRGTAERDPA--YDVVVFENRFPSLAGDSGRCEVVCFTSDHDAS 117
            RTY P  D CPLCPS  G+    P   YDVVVF+NRFP+ +G +G  +VVCFTSDH +S
Sbjct: 61  TRTYKPAVDLCPLCPSVPGSPTEVPEADYDVVVFDNRFPAFSGGTGHADVVCFTSDHHSS 120

Query: 118 FADLSEEQARLVVDAWTDRTSELSHLPSVEQVFCFENRGAEIGVTLGHPHGQIYAYPFTT 177
           FA+L   + R V++A  DRT+ELS    VE VF FENRG EIGVTL HPHGQIYAYPF  
Sbjct: 121 FAELEPRRVRTVLEALADRTAELSVQEGVELVFPFENRGEEIGVTLHHPHGQIYAYPFVP 180

Query: 178 PRTALMLRSLAAHKDATGGGNLFDSVLEEELAGERVVLEGEHWAAFVAYGAHWPYEVHLY 237
           PRT  ML +  AH D  G   L D +  E     R+V EG HW AFV   A WP +V + 
Sbjct: 181 PRTERMLAAARAHHDERGTPLLGDVLASERADRRRIVAEGRHWTAFVPPAAKWPVQVLVV 240

Query: 238 PKRRVPDLLGLDEAARTEFPKVYLELLRRFDRIFGEGEPPTPYIAAWHQAPFGQLEFEGV 297
           P R+VPDL+ L  A R +F  VYL LLR  D ++     P PY+A WHQAP         
Sbjct: 241 PHRQVPDLVELTTAEREDFAAVYLSLLRGCDALY---HRPLPYVAGWHQAPVHH------ 291

Query: 298 TRDDFALHLN-FSLPPYVRQAEVPRGLRIRHE---RVHQRDVPPERAAERLR 345
            RD   LHL  FS    VR+AE         E    V   D  PER AERLR
Sbjct: 292 DRDLAWLHLELFS----VRRAEDKLKYLAGSESGMAVWINDSTPERIAERLR 339


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: 476
Number of extensions: 29
Number of successful extensions: 5
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: 351
Length adjustment: 29
Effective length of query: 325
Effective length of database: 322
Effective search space:   104650
Effective search space used:   104650
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: 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