GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Caulobacter crescentus NA1000

Align Mannose-6-phosphate isomerase; EC 5.3.1.8 (characterized, see rationale)
to candidate CCNA_03732 CCNA_03732 N-acyl-D-glucosamine 2-epimerase

Query= uniprot:P29954
         (387 letters)



>FitnessBrowser__Caulo:CCNA_03732
          Length = 386

 Score =  342 bits (877), Expect = 1e-98
 Identities = 179/370 (48%), Positives = 223/370 (60%), Gaps = 5/370 (1%)

Query: 12  LAGWLNDAALPLWRQKGFDGEGGGFVETIDMKGEPTRDDRRSRVQPRQVYCFAAAGRRGW 71
           L  W  +AA P+W + G D   GGF E ID+ G+     RR RV PRQ+Y +A AG  GW
Sbjct: 15  LKTWAVEAAYPIWWEVGADRVKGGFFEKIDLDGQAVDGPRRGRVLPRQIYAYAIAGDLGW 74

Query: 72  DGDWRTAAEGGLLYFDRVYGQPGGFYGALANADGKLIDASFDLYNQAFALLAFAHLAEVL 131
            G WR A E GL YF   Y +  G +  L   +G+ +D + DLY+QAFAL A A +A+ L
Sbjct: 75  RGPWRAAVEHGLAYFLSAYRRSDGQFRTLVGPNGESLDDTADLYDQAFALFALAAVAKAL 134

Query: 132 PERGAEMVGRSDKLRRQLEARCKHPLAGFEEDDPPRLPLGSNPHMHLFEACLASEEVEGF 191
           P+R  +    +  +R +L A  KHP+AGF + +PP  PL SNPHMHLFEA LA  E++  
Sbjct: 135 PDRADDARTLALVVRERLIAERKHPVAGFHQTNPPSAPLQSNPHMHLFEAMLAWNEID-- 192

Query: 192 DRVAWANLADEIAHLAMDRFIDAESGALREFFDHDWAPFPGEKGRIVEPGHLFEWAWLLL 251
               W  LADEIA LA+ RFI A SG +REFFD DW P PG  GRI EPGH FEW WLL+
Sbjct: 193 KDPIWRTLADEIAELALSRFIHAPSGQIREFFDLDWNPAPGVAGRICEPGHQFEWGWLLM 252

Query: 252 RWAERRGNAQAIVKARRLFEIGEKDGTCPDRDVVVMTLFDDFSVADPTARLWPQTEWLKA 311
           RW +  G A A   A R+ +  E  G    R V +  L DDFS  D  ARLWPQTE +KA
Sbjct: 253 RWGQLAGRADATAAALRMIDDAETHGVDLSRGVAINALLDDFSTHDDGARLWPQTERIKA 312

Query: 312 AIRFAALTEGAERERYLASAGRAAAALQRFLNVPVRGLWRDKQKADGSFVEEPAPASTFY 371
           A+  A +T  A   RY   A  AA  L  +L   + GLWRDK + D +F+EEP PAS+FY
Sbjct: 313 AVLAAEITGQA---RYWDMAAAAAEGLMAYLRTAIPGLWRDKYQPDETFIEEPVPASSFY 369

Query: 372 HILCAIYELE 381
           HI  AI E++
Sbjct: 370 HIALAILEMD 379


Lambda     K      H
   0.323    0.139    0.448 

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: 484
Number of extensions: 18
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: 387
Length of database: 386
Length adjustment: 30
Effective length of query: 357
Effective length of database: 356
Effective search space:   127092
Effective search space used:   127092
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 (21.9 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