GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galE in Synechococcus elongatus PCC 7942

Align UDP-glucose 4-epimerase; UDP-galactose 4-epimerase; Uridine diphosphate galactose 4-epimerase; EC 5.1.3.2 (characterized)
to candidate Synpcc7942_1149 Synpcc7942_1149 dTDP-glucose 46-dehydratase

Query= SwissProt::A0R5C5
         (313 letters)



>FitnessBrowser__SynE:Synpcc7942_1149
          Length = 325

 Score =  141 bits (355), Expect = 2e-38
 Identities = 100/318 (31%), Positives = 153/318 (48%), Gaps = 15/318 (4%)

Query: 1   MRTLVTGAAGFIGSTLVDRLLADGHGVVGLDDLSSGRAENLHSAENSDKFEFVKADIVDA 60
           MR LVTG AGFIGS L+DRL++ GH V+ LD+  +GR  N+       +FE ++ DI D 
Sbjct: 2   MRILVTGGAGFIGSHLIDRLMSAGHEVICLDNYFTGRKHNVAQWYGHPRFELIRHDITDP 61

Query: 61  DLTGLLAEFKPEVIFHLAAQISVKRSVDDPPFDATVNVVGTVRLAEAARLAGVRKVVHTS 120
                    + + I+HLA   S      +P   A  + +GTV +   A+    R ++ ++
Sbjct: 62  ------IRLEVDQIYHLACPASPVHYQYNPIKTAKTSFLGTVNMLGLAKRVKARLLMAST 115

Query: 121 SGGSVYGTPPAYPTSEDM-----PVNPASPYAAGKVAGEVYLNMYRNLYDLDCSHIAPAN 175
           S   VYG P  +P +ED      P+   S Y  GK   E     Y   ++L+       N
Sbjct: 116 S--EVYGDPHVHPQTEDYWGNVNPIGIRSCYDEGKRVAETLCFDYHRQHNLEIRVARIFN 173

Query: 176 VYGPRQDPHGEAGVVAIFSEALLAGRTTKIFGDGSDTRDYVFVDDVVDAFVRAGGPAGGG 235
            YGPR     +  VV+ F    L G+   ++G G  TR + +V D+VD  +R       G
Sbjct: 174 TYGPRM-LENDGRVVSNFIVQALQGQPLTVYGRGEQTRSFCYVSDLVDGLIRLMNGDHLG 232

Query: 236 QRFNVGTGVETSTRELHTAIAGAVGAPDEPEFHPPRLGDLRRSRLDNTRAREVLGWQPQV 295
              N+G   E +  +L   I   +      EF P    D ++ R D +RA+  L WQP V
Sbjct: 233 P-VNLGNPSEYTILQLAELIRDRIDPALPIEFRPLPQDDPQQRRPDISRAQAWLKWQPLV 291

Query: 296 ALAEGIAKTVEFFRNKSQ 313
           ++ +G+ +T+  FR++ Q
Sbjct: 292 SVQDGLDRTIADFRDRQQ 309


Lambda     K      H
   0.317    0.136    0.396 

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: 253
Number of extensions: 14
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: 313
Length of database: 325
Length adjustment: 28
Effective length of query: 285
Effective length of database: 297
Effective search space:    84645
Effective search space used:    84645
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 (21.6 bits)
S2: 48 (23.1 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