Align Putative succinate-semialdehyde dehydrogenase [NADP(+)] 2; SSADH 2; SSDH 2; EC 1.2.1.79 (characterized)
to candidate WP_052591203.1 VV02_RS09505 succinate-semialdehyde dehydrogenase (NADP(+))
Query= SwissProt::P9WNX7 (518 letters) >NCBI__GCF_001190945.1:WP_052591203.1 Length = 535 Score = 482 bits (1241), Expect = e-140 Identities = 247/472 (52%), Positives = 319/472 (67%) Query: 34 TGKPLTTIPVGTAADVEAAFAEARAAQTDWAKRPVIERAAVIRRYRDLVIENREFLMDLL 93 TG L +PV T V+ A+ AR AQ WA +P+ RA V+ R DLV N+ L+DL+ Sbjct: 52 TGGHLADLPVSTIDSVDHAYRSAREAQARWASQPIAARARVLLRLHDLVFRNQNELLDLI 111 Query: 94 QAEAGKARWAAQEEIVDLIANANYYARVCVDLLKPRKAQPLLPGIGKTTVCYQPKGVVGV 153 Q E+GK R A EEI+D+ +YAR LKPRK +P + +T PKGVVGV Sbjct: 112 QLESGKTRGQAFEEILDVAGVCRHYARKAEHYLKPRKRLGAIPVLTQTVELRHPKGVVGV 171 Query: 154 ISPWNYPMTLTVSDSVPALVAGNAVVLKPDSQTPYCALACAELLYRAGLPRALYAIVPGP 213 ++PWNYP++++V+D +PAL+AGNAVV++PD ++ AL ELL +AGLP L +V G Sbjct: 172 VAPWNYPLSMSVTDLIPALLAGNAVVVRPDEKSALTALRSFELLDQAGLPEGLLQVVLGD 231 Query: 214 GSVVGTAITDNCDYLMFTGSSATGSRLAEHAGRRLIGFSAELGGKNPMIVARGANLDKVA 273 G +G A+ D DY+MFTGS+ATG +A AG RL+G S ELGGKN M +A ANL A Sbjct: 232 GPTIGKAVLDRADYVMFTGSTATGRTVARDAGERLVGASLELGGKNAMYIAADANLKAAA 291 Query: 274 KAATRACFSNAGQLCISIERIYVEKDIAEEFTRKFGDAVRNMKLGTAYDFSVDMGSLISE 333 A R+ FS+AGQLCISIER+ + + IA+EF F VR MK+G + MGSLIS+ Sbjct: 292 DCAVRSVFSSAGQLCISIERLILHEAIADEFLTHFIKRVRAMKIGPDLAWGNTMGSLISQ 351 Query: 334 AQLKTVSGHVDDATAKGAKVIAGGKARPDIGPLFYEPTVLTNVAPEMECAANETFGPVVS 393 AQL V+ HV+DA AKGA V+AGG+ARP++GP FYEPTVL V M C ETFGPVVS Sbjct: 352 AQLDKVTEHVEDARAKGATVLAGGRARPELGPYFYEPTVLEGVTAAMTCRDEETFGPVVS 411 Query: 394 IYPVADVDEAVEKANDTDYGLNASVWAGSTAEGQRIAARLRSGTVNVDEGYAFAWGSLSA 453 +Y V+ DEAV ANDT YGLNASV+ + G+ +AAR+++GTVNV+EGY AWGS + Sbjct: 412 VYRVSTDDEAVALANDTSYGLNASVFTKDISRGRGLAARIKAGTVNVNEGYVSAWGSNGS 471 Query: 454 PMGGMGLSGVGRRHGPEGLLKYTESQTIATARVFNLDPPFGIPATVWQKSLL 505 PMGGM SGVGRRHG EG+ KYTESQT+A + + P G+P +W KS++ Sbjct: 472 PMGGMRQSGVGRRHGAEGIWKYTESQTVAVQHLMPIAPTKGVPEKLWAKSMV 523 Lambda K H 0.318 0.134 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: 692 Number of extensions: 22 Number of successful extensions: 1 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: 518 Length of database: 535 Length adjustment: 35 Effective length of query: 483 Effective length of database: 500 Effective search space: 241500 Effective search space used: 241500 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 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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:
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