GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manA in Lacinutrix himadriensis E4-9a

Align Mannose-6-phosphate isomerase ManA; Phosphohexomutase; Phosphomannose isomerase; PMI; EC 5.3.1.8 (characterized)
to candidate WP_083478354.1 AMD28_RS16110 mannose-6-phosphate isomerase

Query= SwissProt::O31646
         (315 letters)



>NCBI__GCF_001418105.1:WP_083478354.1
          Length = 324

 Score =  189 bits (481), Expect = 6e-53
 Identities = 112/316 (35%), Positives = 175/316 (55%), Gaps = 19/316 (6%)

Query: 1   MTTEPLFFKPVFKERIWGGTALADFGYTIPSQRT-----GECWAFAAHQNGQSVVQNGMY 55
           M T P+ F+P+ KE+IWGG  L    +T+  + +     GE W  +   +  S+V NG+ 
Sbjct: 4   MLTYPIKFEPILKEKIWGGQKL----HTLLKKESALPNIGESWEISDVDHDISIVNNGVL 59

Query: 56  KGFTLSELWEHHR-HLFG----QLEGDRFPLLTKILDADQDLSVQVHPNDEYANIHENGE 110
           KG TL EL E ++  L G    Q  G+ FPLL K +DA +DLS+Q+HPND  A+   N  
Sbjct: 60  KGKTLKELLETYKADLIGNKNYQAFGNTFPLLIKFIDAKEDLSIQLHPNDALASKRHNS- 118

Query: 111 LGKTECWYIIDCQKDAEIIYGHNAT-TKEELTTMIERGEWDELLRRVKVKPGDFFYVPSG 169
            GKTE WY++  + DA +I G N   T E+    +E     E+L   KVK GD ++V  G
Sbjct: 119 FGKTEMWYVLQAEDDARLIVGFNQEMTSEKYVKHLEAKTLPEILNFDKVKEGDSYFVEVG 178

Query: 170 TVHAIGKGILALETQQNSDTTYRLYDYDRKDAEGKLRELHLKKSIEVIEVPSIPERHTVH 229
            +HAIG G++  E QQ SD TYR+YD+DR D+ G  RELH   +I+ I   S  E   V 
Sbjct: 179 QIHAIGAGVMLAEIQQTSDVTYRIYDWDRVDSNGNQRELHNDLAIDAINFKS-QEDFKVS 237

Query: 230 HEQIEDLLTTTLIECAYFSVGKWNLSGSASLKQQ-KPFLLISVIEGEGRMISGEYVYPFK 288
           + + E+     +++C YF+     ++ + + + +   F++   + GE  +++  +    K
Sbjct: 238 YSKAEN-EANEMVDCPYFTCNYIEITETINKENKVDSFIIYMCVSGEVEIVTAHHTVKIK 296

Query: 289 KGDHMLLPYGLGEFKL 304
           KG+ +LLP  +  +++
Sbjct: 297 KGETVLLPAAIKTYQI 312


Lambda     K      H
   0.319    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: 286
Number of extensions: 19
Number of successful extensions: 6
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: 315
Length of database: 324
Length adjustment: 28
Effective length of query: 287
Effective length of database: 296
Effective search space:    84952
Effective search space used:    84952
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 (21.7 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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